Hydrochloric Acid → 4,4-Dimethylcyclohexanecarboxylic acid

HRID 2055179노트

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HRID 2055179 반응식
[CH3:1][C:2]1([CH3:14])[CH2:7][CH2:6]C(=C2SCCCS2)[CH2:4][CH2:3]1.[C:15]([OH:21])([C:17](F)(F)F)=[O:16].OO.[OH-].[Na+].Cl>C(#N)C.ClCCl.O>[CH3:1][C:2]1([CH3:14])[CH2:7][CH2:6][CH:17]([C:15]([OH:21])=[O:16])[CH2:4][CH2:3]1

참가 물질

9

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온도
80 °C

실험 절차

2-(4,4-Dimethyl-cyclohexylidene)-[1,3]dithiane (21.6 g, 95 mmol) and TFA (30.5 mL, 0.32 mol) were placed in acetonitrile (100 mL) and water (25 mL) and the mixture was heated at 65° C. for 3 h. 30% Aqueous hydrogen peroxide (152 mL, 1.3 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, 630 mL). The resulting mixture was cooled to 0° C. and acidified with aqueous 6N HCl. Dichloromethane (500 mL) was added and the mixture was filtered. The aqueous phase was extracted with dichloromethane (100 mL×5), was dried (MgSO4) and was evaporated in vacuo to yield the title compound (12 g, 81%). MH+157.

후처리

  1. temperaturethe reaction mixture was cooled to 40° C.
  2. temperatureThe resulting mixture was cooled to 0° C.
  3. filtrationthe mixture was filtered
  4. extractionThe aqueous phase was extracted with dichloromethane (100 mL×5)
  5. dry with materialwas dried (MgSO4)
  6. customwas evaporated in vacuo

출처 및 근거

ORD 기록
ord-c0f0aef98538417993a0df2a89a2bada
출처 데이터셋
uspto-grants-2008_02
특허 번호
US07332485B2

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