Nitric Acid → 1,1,1,4,4,4-Hexafluorobutane

HRID 1379918

반응식

HRID 1379918 반응식
[N+]([O-])(O)=O.[F:5][C:6]([F:14])([F:13])[CH:7]=[CH:8][C:9]([F:12])([F:11])[F:10].[H][H]>>[F:5][C:6]([F:14])([F:13])[CH2:7][CH2:8][C:9]([F:12])([F:11])[F:10]

참가 물질

4

반응물 3

HCID 944Nitric AcidHCID 27749751,1,1,4,4,4-Hexafluoro-2-buteneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 678901,1,1,4,4,4-Hexafluorobutane수율 99%

실험 절차

In a 20 1 stainless steel autoclave, which had previously been conditioned using 10% strength nitric acid and was equipped with closed circuit heating and an anchor stirrer, 10.0 kg of 1,1,1,4,4,4-hexafluorobutene were heated from 0 to 30 C. over a period of 10 minutes in the presence of 250 g of catalyst (5% by weight of metallic palladium on activated carbon) at a pressure of 20 bar of hydrogen. After reaching this temperature, the hydrogen consumption was compensated for by repeated pressurization with fresh hydrogen at pressures between 20 and 30 bar. After about 2.5 hours the conversion was 87%. 1,1,1,4,4,4-Hexafluorobutane had been formed in a yield of greater than 99% of theory.

후처리

  1. customwas equipped
  2. customwith closed circuit
  3. temperatureheating
  4. customthe hydrogen consumption

출처 및 근거

ORD 기록
ord-dd800c5757ae4403aac47100bbb57a5e
출처 데이터셋
uspto-grants-1997_09
특허 번호
US05672787

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