Processes for the preparation of 2-chloro-1,1,1,2,3,3,3-heptafluoropropane, hexafluoropropene and 1,1,1,2,3,3,3-heptafluoropropane
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C07C-017/00
C07C-017/266
C07C-017/10
출원번호
US-0523223
(2003-08-21)
우선권정보
US-60/405222(2002-08-22)
국제출원번호
PCT/US03/026331
(2003-08-21)
§371/§102 date
20050131
(20050131)
국제공개번호
WO04/018397
(2004-03-04)
발명자
/ 주소
Nappa,Mario J.
Rao,Velliyur Nott Mallikarjuna
Rosenfeld,H. David
Subramoney,Sekhar
Subramanian,Munirpallam A.
Sievert,Allen C.
출원인 / 주소
E. I. du Pont de Nemours and Company
인용정보
피인용 횟수 :
8인용 특허 :
6
초록▼
A process for the preparation of 2-chloro-1,1,1,3,3,3-heptafluoropropane is disclosed which involves (a) contacting a mixture comprising hydrogen fluoride, chlorine, and at least one starting material selected from the group consisting of halopropenes of the formula CX3CCI═CX2 and halopropanes
A process for the preparation of 2-chloro-1,1,1,3,3,3-heptafluoropropane is disclosed which involves (a) contacting a mixture comprising hydrogen fluoride, chlorine, and at least one starting material selected from the group consisting of halopropenes of the formula CX3CCI═CX2 and halopropanes of the formula the CX3CCIYCX3, wherein each X is independently F or Cl, and Y is H, Cl or F (provided that the number of X and Y which are F totals no more than six) with a chlorofluorination catalyst in a reaction zone to produce a product mixture comprising CF3CCIFCF3, HCI, HF. and underfluorinated halogenated hydrocarbon intermediates. The process is characterized by said chlorofluorination catalyst comprising at least one chromium-containing component selected from (i) a crystalline alpha-chromium oxide where at least 0.05 atom % of the chromium atoms in the alpha-chromium oxide lattice are replaced by nickel, trivalent cobalt or both nickel and trivalent cobalt, provided that no more than 2 atom % of the chromium atoms in the alpha-chromium oxide lattice are replaced by nickel and that the total amount of chromium atoms in the alpha-chromium oxide lattice that are replaced by nickel and trivalent cobalt is no more than 6 atom %, and (ii) a fluorinated crystalline oxide of (i). Also disclosed is a process for the manufacture of a mixture of HFC-227ea and hexafluoropropene by reacting a starting mixture comprising CFC-217ba and hydrogen in the vapor phase at an elevated temperature, optionally in the presence of a hydrogenation catalyst. This process involves preparing the CFC-217ba by the process described above.
대표청구항▼
What is claimed is: 1. A process for the preparation of 2-chloro-1,1,1,2,3,3,3-heptafluoropropane, comprising: (a) contacting a mixture comprising hydrogen fluoride, chlorine, and at least one starting material selected from the group consisting of halopropenes of the formula CX3CCl═CX2 and h
What is claimed is: 1. A process for the preparation of 2-chloro-1,1,1,2,3,3,3-heptafluoropropane, comprising: (a) contacting a mixture comprising hydrogen fluoride, chlorine, and at least one starting material selected from the group consisting of halopropenes of the formula CX3CCl═CX2 and halopropanes of the formula the CX3CClYCX3, wherein each X is independently selected from the group consisting of F and Cl, and Y is selected from the group consisting of H, Cl and F, provided that the number of X and Y which are F totals no more than six, with a chlorofluorination catalyst in a reaction zone to produce a product mixture comprising CF3CClFCF3, HCl, HF, and underfluorinated halogenated hydrocarbon intermediates; wherein said chlorofluorination catalyst comprises at least one chromium-containing component selected from (i) a crystalline alpha-chromium oxide where at least 0.05 atom % of the chromium atoms in the alpha-chromium oxide lattice are replaced by nickel, trivalent cobalt or both nickel and trivalent cobalt, provided that no more than 2 atom % of the chromium atoms in the alpha-chromium oxide lattice are replaced by nickel and that the total amount of chromium atoms in the alpha-chromium oxide lattice that are replaced by nickel and trivalent cobalt is no more than 6 atom %, and (ii) a fluorinated crystalline oxide of (i). 2. The process of claim 1 further comprising (b) separating the product of step (a) to recover CF3 CClFCF3 as a product and to obtain underfluorinated halogenated hydrocarbon intermediates; and (c) returning underfluorinated halogenated hydrocarbon intermediates obtained in step (b) back to the step (a) reaction zone. 3. A process for the manufacture of a mixture of CF3 CHFCF3 and CF2═CFCF3 by reacting a starting mixture comprising CF3CClFCF3 and hydrogen in the vapor phase at an elevated temperature, optionally in the presence of a hydrogenation catalyst, characterized by preparing the CF3 CClFCF3 by the process of claim 1.
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이 특허에 인용된 특허 (6)
Manogue William H. (Newark DE) Rao Velliyur N. M. (Wilmington DE), Halocarbon hydrogenolysis.
Webster James L. (Parkersburg WV) McCann Elrey L. (Mendenhall PA) Bruhnke Douglas W. (Landenberg PA) Lerou Jan J. (Chadds Ford PA) Manogue William H. (Newark DE) Manzer Leo E. (Wilmington DE) Swearin, Multistep synthesis of hexafluoropropylene.
Webster James L. (Parkersburg WV) McCann Elrey L. (Mendenhall PA) Bruhnke Douglas W. (Landenberg PA) Lerou Jan J. (Chadds Ford PA) Manzer Leo E. (Wilmington DE) Manogue William H. (Newark DE) Resnick, Multistep synthesis of hexafluoropropylene.
Webster James L. (Parkersburg WV) Trofimenko Swiatoslaw (Wilmington DE) Resnick Paul R. (Wilmington DE) Bruhnke Douglas W. (Landenberg PA) Lerou Jan J. (Chadds Ford PA) Manogue William H. (Newark DE), Multistep synthesis of hexafluoropropylene.
Gumprecht William H. (Wilmington DE) Manzer Leo E. (Wilmington DE) Rao V. N. Mallikarjuna (Wilmington DE), Process for the manufacture of 1,1,1-trifluorodichloroethane and 1,1,1,2-tetrafluorochloroethane.
Rao, Velliyur Nott Mallikarjuna; Rosenfeld, H. David; Sievert, Allen Capron; Subramoney, Shekhar, Process for the preparation of 1,1,1,3,3-penta-fluoropropane and/or 1,1,1,3,3,3-hexafluoropropane.
Rao, Velliyur Nott Mallikarjuna; Rosenfeld, H. David; Sievert, Allen Capron; Subramoney, Shekhar, Process for the preparation of 1,1,1,3,3-pentafluoropropane and 1,1,1,2,3-pentafluoropropane.
Rao, Velliyur Nott Mallikarjuna; Rosenfeld, H. David; Sievert, Allen Capron; Subramoney, Shekhar, Process for the preparation of 1,1,3,3,3-pentafluoropropene and 1,2,3,3,3-pentafluoropropene.
Rao, Velliyur Nott Mallikarjuna; Rosenfeld, H. David; Sievert, Allen Capron; Subramoney, Shekhar, Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 1,1,3,3,3-pentafluoropropene.
Rao, Velliyur Nott Mallikarjuna; Rosenfeld, H. David; Sievert, Allen Capron; Subramoney, Shekhar, Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 2,3,3,3-tetrafluoropropene.
Rao, Velliyur Nott Mallikarjuna; Rosenfeld, H. David; Sievert, Allen Capron; Subramoney, Shekhar, Process or the preparation of 1,1,1,3,3,3-hexafluoro-propane and at least one of 1,1,1,2,3,3-hexafluoropropane, hexafluoropropane and 1,1,1,2,3,3,3-heptafluoropropane.
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