홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

p-Toluenesulfonic acid monohydrate → 4-Methoxy-4-(trifluoromethyl)cyclohexan-1-one

HRID 922120
노트
인쇄 미리보기

반응식

HRID 922120 반응식
[CH3:1][O:2][C:3]1([C:13]([F:16])([F:15])[F:14])[CH2:12][CH2:11][C:6]2(OCC[O:7]2)[CH2:5][CH2:4]1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CC(C)=O.O>[CH3:1][O:2][C:3]1([C:13]([F:14])([F:15])[F:16])[CH2:4][CH2:5][C:6](=[O:7])[CH2:11][CH2:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 712468178-Methoxy-8-(trifluoromethyl)-1,4-dioxaspiro[4.5]decane

생성물 1

HCID 894014664-Methoxy-4-(trifluoromethyl)cyclohexan-1-one

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매2회

실험 절차

11.80 g (49.12 mmol) of 8-methoxy-8-(trifluoromethyl)-1,4-dioxaspiro[4.5]decane (Example 9A) were dissolved in 236 ml of acetone and 118 ml of water, 1.50 g (7.86 mmol) of 4-toluenesulphonic acid monohydrate were added and the mixture was heated at reflux overnight. The mixture was then poured into 1.2 l of water and the product was extracted with diethyl ether. The organic phase was washed with water, dried over sodium sulphate and concentrated under reduced pressure. The resulting residue was distilled under reduced pressure (boiling point: 106-110° C. at 40 mbar). This gave 6.86 g (71% of theory) of the title compound as a yellowish oil.

후처리

  1. temperaturethe mixture was heated
  2. temperatureat reflux overnight
  3. extractionthe product was extracted with diethyl ether
  4. washThe organic phase was washed with water
  5. dry with materialdried over sodium sulphate
  6. concentrationconcentrated under reduced pressure
  7. distillationThe resulting residue was distilled under reduced pressure (boiling point: 106-110° C. at 40 mbar)

출처 및 근거

ORD 기록
ord-85c9c50769a94a8da60ee05842c2430a
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278925B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트