2-Hexanone → Phenylmethoxy-2,4-octandione

HRID 274594노트

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HRID 274594 반응식
[CH3:1][C:2](=[O:7])[CH2:3][CH2:4][CH2:5][CH3:6].[NH2-].[Na+].[C:10]1([CH2:16][O:17][CH2:18][C:19](OC)=[O:20])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>CCOCC>[C:10]1([CH2:16][O:17][CH2:18][C:19](=[O:20])[CH2:1][C:2](=[O:7])[CH2:3][CH2:4][CH2:5][CH3:6])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

참가 물질

5

실험 절차

2-Hexanone (26.7 g) was added dropwise over 5 min at room temperature to a stirred suspension of sodium amide (10.4 g) in dry ether (290 ml) under nitrogen. The reaction mixture was stirred for 13 min. and a solution of methyl phenylmethoxyacetate (24.0 g) in dry ether (40 ml) was added dropwise over 12 min. The mixture was then heated at reflux for 3 h, cooled, and then poured into ice (400 g) and 2N HC1 (200 ml). The aqueous phase was extracted with ether (2×350 ml) and the combined etheral solution washed with 8% sodium bicarbonate solution (2×250 ml), water (200 ml) and brine (200 ml), then dried and evaporated to leave a yellow liquid (35.8 g). This was purified by column chromatography on silica gel eluting with System A (2:98) to give the title compound as a yellow oil (10.95 g).

후처리

  1. temperatureThe mixture was then heated
  2. temperatureat reflux for 3 h
  3. temperaturecooled
  4. extractionThe aqueous phase was extracted with ether (2×350 ml)
  5. washthe combined etheral solution washed with 8% sodium bicarbonate solution (2×250 ml), water (200 ml) and brine (200 ml)
  6. customdried
  7. customevaporated

출처 및 근거

ORD 기록
ord-8ea49cbb94574cde831c0e8b4f6c7351
출처 데이터셋
uspto-grants-1995_02
특허 번호
US05389659

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