Isopropenyl chloroformate → Prop-1-en-2-yl (1-methoxycyclopropane-1-carbonyl)carbamate

HRID 626531노트

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HRID 626531 반응식
[CH3:1][O:2][C:3]1([C:6]([NH2:8])=[O:7])[CH2:5][CH2:4]1.C[Si]([N-][Si](C)(C)C)(C)C.[Li+].Cl[C:20]([O:22][C:23]([CH3:25])=[CH2:24])=[O:21]>C1COCC1>[CH3:1][O:2][C:3]1([C:6]([NH:8][C:20](=[O:21])[O:22][C:23]([CH3:25])=[CH2:24])=[O:7])[CH2:5][CH2:4]1

참가 물질

5

실험 절차

A −78° C. solution of 1-methoxycyclopropane-1-carboxamide (0.23 g, 1.998 mmol) in THF (6 mL) was treated drop-wise with lithium bis(trimethylsilyl)amide (1M THF, 2.80 mL, 2.80 mmol), stirred for 0.5 h, treated drop-wise with a solution of isopropenyl chloroformate (0.262 mL, 2.397 mmol) in dry THF (1 mL), stirred for 1 h at −78° C., allowed to slowly warm to RT and stirred for 1 h. The mixture was quenched with satd. NaHCO3), extracted with EtOAc (3×) and the combined organics were dried over Na2SO4 and concentrated to dryness to afford prop-1-en-2-yl (1-methoxycyclopropane-1-carbonyl)carbamate (0.423 g, 106%). MS(ESI) m/z: 222.1 (M+Na+).

후처리

  1. stirringstirred for 1 h at −78° C.
  2. stirringstirred for 1 h
  3. customThe mixture was quenched with satd
  4. extractionNaHCO3), extracted with EtOAc (3×)
  5. dry with materialthe combined organics were dried over Na2SO4
  6. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-e66841940c1e4940ba5795fc85061200
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09309224B2

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