Hydrochloric Acid → cis-3,5-Dimethylcyclohexane-1-carboxylic acid

HRID 2055195노트

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HRID 2055195 반응식
[CH3:1][C@H:2]1[CH2:7][C@@H](C)[CH2:5][C:4](=[C:9]2SCCCS2)[CH2:3]1.[C:15]([OH:21])([C:17](F)(F)F)=[O:16].OO.[OH-].[Na+].Cl>C(#N)C.O>[CH3:1][C@H:2]1[CH2:3][C@@H:4]([CH3:9])[CH2:5][CH:17]([C:15]([OH:21])=[O:16])[CH2:7]1

참가 물질

8

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온도
80 °C

실험 절차

2-((3S,5R)-3,5-Dimethyl-cyclohexylidene)-[1,3]dithiane (8.36 g, 0.036 mmol) and TFA (9.5 mL, 0.12 mol) were placed in acetonitrile (480 mL) and water (120 mL) and the mixture was heated at 65° C. for 1 h. 30% Aqueous hydrogen peroxide (48 mL, 0.49 mol) was added carefully and the mixture was warmed to 80° C. slowly. After 1 h, the reaction mixture was cooled to 40° C. and was added slowly to an aqueous solution of NaOH (6N, 475 mL). The resulting mixture was cooled to 0° C. and acidified with aqueous 6N HCl. The acetonitrile was removed by rotary evaporation. The residue was extracted with dichloromethane (100 mL×5) was dried (MgSO4) and was evaporated in vacuo to yield the title compound as a white wax (4.1 g, 72%). MH+157.

후처리

  1. temperaturethe reaction mixture was cooled to 40° C.
  2. temperatureThe resulting mixture was cooled to 0° C.
  3. customThe acetonitrile was removed by rotary evaporation
  4. extractionThe residue was extracted with dichloromethane (100 mL×5)
  5. dry with materialwas dried (MgSO4)
  6. customwas evaporated in vacuo

출처 및 근거

ORD 기록
ord-4fdd8f6388ac42c6aab3776346f75e86
출처 데이터셋
uspto-grants-2008_02
특허 번호
US07332485B2

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