Sodium hydride → 1-Benzhydryl-3-(methoxymethylene)azetidine

HRID 28474

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HRID 28474 반응식
[H-].[Na+].[Cl-].[CH3:4][O:5][CH2:6][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[CH:26]([N:39]1[CH2:42][C:41](=O)[CH2:40]1)([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>O1CCCC1>[CH:26]([N:39]1[CH2:42][C:41](=[CH:4][O:5][CH3:6])[CH2:40]1)([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

참가 물질

5

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온도
0 °C

실험 절차

To a suspension of sodium hydride (60% mineral oil dispersion, 0.10 g, 2.3 mmol) in anhydrous tetrahydrofuran (30 mL) was added (methyoxymethyl)triphenylphosphonium chloride (0.80 g, 2.3 mmol) at 0° C. The mixture was stirred at 0° C. for 40 minutes, then a solution of 1-benzhydryl-azetidin-3-one (0.50 g, 2.1 mmol) in tetrahydrofuran was introduced at 0° C. The resulting mixture was refluxed for 2 hours. The reaction was quenched with water and extracted with methylene chloride (3×50 mL). The organic layer was washed with water (3×50 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The crude oil was column chromatographed on silica gel (20% ethyl acetate-hexane). The product-containing fractions were concentrated under vacuum to give 0.29 g (52%) of the title compound as a light yellow solid, m.p. 56-58° C.

후처리

  1. temperatureThe resulting mixture was refluxed for 2 hours
  2. customThe reaction was quenched with water
  3. extractionextracted with methylene chloride (3×50 mL)
  4. washThe organic layer was washed with water (3×50 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuum
  8. customchromatographed on silica gel (20% ethyl acetate-hexane)
  9. concentrationThe product-containing fractions were concentrated under vacuum

출처 및 근거

ORD 기록
ord-3fd7fe6359cb45f0a0d22f0fc75f564a
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07419986B2

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