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Acetic Acid → Methyl 2-methoxyimino-2-(3-hydroxyphenyl)acetate

HRID 1065868
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HRID 1065868 반응식
[N+:1](=[CH2:3])=[N-].[C:4](O)(=[O:6])C.[CH:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[C:14]([O:17][CH2:18]C)(=[O:16])C.CC[O:22]CC>>[CH3:4][O:6][N:1]=[C:3]([C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([OH:22])[CH:9]=1)[C:14]([O:17][CH3:18])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 176Acetic AcidHCID 241BenzeneHCID 3283Diethyl Ether2회HCID 8857Ethyl AcetateHCID 9550Diazomethane

생성물 1

HCID 54365989Methyl 2-methoxyimino-2-(3-hydroxyphenyl)acetate

실험 절차

This material was dissolved in ether (60 ml.) and a solution of diazomethane in ether was gradually added thereto under ice-cooling until the color of the mixture was changed to yellow. Acetic acid was immediately added thereto and the mixture was washed with a sodium bicarbonate aqueous solution and a saturated sodium chloride aqueous solution and dried over magnesium sulfate. Ether was distilled off to give oily residue (10.8 g.). The oily residue was subjected to column chromatography on silica gel (165 g.) using a mixture of benzene and ethyl acetate (9:1) as developing solvent. Firstly the eluate containing syn isomer was eluted and the eluate was collected and concentrated to give oily methyl 2-methoxyimino-2-(3-hydroxyphenyl)acetate (syn isomer) (7.9 g.). The oil was allowed to stand to give crystals, mp 39.5° to 40.5° C.

후처리

  1. temperatureunder ice-cooling until the color of the mixture
  2. washthe mixture was washed with a sodium bicarbonate aqueous solution
  3. dry with materiala saturated sodium chloride aqueous solution and dried over magnesium sulfate
  4. distillationEther was distilled off
  5. customto give oily residue (10.8 g.)
  6. additionFirstly the eluate containing syn isomer
  7. washwas eluted
  8. customthe eluate was collected
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1ea9945caf244c40a963bae10ac76024
출처 데이터셋
uspto-grants-1982_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04331664

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