Oxalyl chloride → HCID 19835291, 화합물

HRID 477963

반응식

HRID 477963 반응식
[CH:1]1([CH:7]2[CH2:12][CH2:11][CH:10]([C:13]([OH:15])=O)[CH2:9][CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(Cl)(=O)C(Cl)=O.Cl.[CH3:23][NH:24][OH:25]>O1CCCC1.CN(C)C=O.[OH-].[Na+]>[CH:1]1([CH:7]2[CH2:12][CH2:11][CH:10]([C:13]([N:24]([OH:25])[CH3:23])=[O:15])[CH2:9][CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

참가 물질

7

실험 절차

To a solution of 4-cyclohexyl-cyclohexanecarboxylic acid (1.47 g, 7 mmol) in 50 ml of tetrahydrofuran was added oxalyl chloride (0.67 ml, 7.7 mmol) and a few drops of dimethylformamide. After stirring for one hour, the reaction mixture was concentrated to about 1/3 of the original volume and added dropwise into a cold (~0° C.), stirred solution of N-methylhydroxylamine hydrochloride (1.17 g, 14 mmol) in 40 ml of 1N sodium hydroxide. The mixture was stirred for two hours and extracted three times with ethyl acetate. The combined ethyl acetate extracts were washed twice with water, dried with anhydrous sodium sulfate and concentrated. Purification by flash chromatography and crystallization afforded 0.342 g of 4-cyclohexyl-N-hydroxy-N-methylcyclohexanecarboxamide as a white solid (m.p. 89°-90° C.).

후처리

  1. concentrationthe reaction mixture was concentrated to about 1/3 of the original volume
  2. additionadded dropwise into a cold (~0° C.)
  3. stirringThe mixture was stirred for two hours
  4. extractionextracted three times with ethyl acetate
  5. washThe combined ethyl acetate extracts were washed twice with water
  6. dry with materialdried with anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customPurification
  9. customby flash chromatography and crystallization

출처 및 근거

ORD 기록
ord-19b7ee22410040a3bdf1d114a7a46b5d
출처 데이터셋
uspto-grants-1989_12
특허 번호
US04889874

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