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Hydrochloric Acid → 4,5,5-Trifluoro-2-(prop-2-EN-1-YL)pent-4-EN-1-OL

HRID 1987443
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인쇄 미리보기

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HRID 1987443 반응식
[C:1](=[C:4]([CH2:6][CH:7]([CH2:13][CH:14]=[CH2:15])[CH2:8][O:9]COC)[F:5])([F:3])[F:2].CO.Cl>O>[C:1](=[C:4]([CH2:6][CH:7]([CH2:13][CH:14]=[CH2:15])[CH2:8][OH:9])[F:5])([F:3])[F:2]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 714163061,1,2-Trifluoro-4-[(methoxymethoxy)methyl]hepta-1,6-diene

생성물 1

HCID 714163054,5,5-Trifluoro-2-(prop-2-EN-1-YL)pent-4-EN-1-OL수율 109.8%

시약·촉매·용매 1

HCID 962Water용매

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온도
60 °C

실험 절차

40 g of CF2═CFCH2CH(CH2OCH2OCH3)CH2CH═CH2 obtained in Example 3 and 100 mL of methanol were put into a 300 mL glass reactor, and a catalytic amount of concentrated hydrochloric acid was added thereto, followed by heating at 60° C. for 19 hours. The reaction solution was cooled to room temperature, and 30 mL of water was added to carry out liquid separation. The organic layer was further washed with 50 mL of water and subjected to precision distillation to obtain 35.3 g of CF2═CFCH2CH(CH2OH)CH2CH═CH2 (59-60° C./0.5 kPa).

후처리

  1. temperatureThe reaction solution was cooled to room temperature
  2. customliquid separation
  3. washThe organic layer was further washed with 50 mL of water
  4. distillationsubjected to precision distillation

출처 및 근거

ORD 기록
ord-363678c7d2b34e12988f014078f041d8
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07550545B2

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