Chloromethyl chloroformate → Chloromethyl cyclopropyl(4-methyl-3-nitrobenzoyl)carbamate

HRID 2100364

반응식

HRID 2100364 반응식
[CH:1]1([NH:4][C:5](=[O:16])[C:6]2[CH:11]=[CH:10][C:9]([CH3:12])=[C:8]([N+:13]([O-:15])=[O:14])[CH:7]=2)[CH2:3][CH2:2]1.C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[C:27](Cl)(=[O:31])[O:28][CH2:29][Cl:30]>C1COCC1>[CH:1]1([N:4]([C:5](=[O:16])[C:6]2[CH:11]=[CH:10][C:9]([CH3:12])=[C:8]([N+:13]([O-:15])=[O:14])[CH:7]=2)[C:27](=[O:31])[O:28][CH2:29][Cl:30])[CH2:3][CH2:2]1

참가 물질

5

반응물 3

HCID 62754Chloromethyl chloroformateHCID 2162665N-cyclopropyl-4-methyl-3-nitrobenzamideHCID 2733832Lithium Hexamethyldisilazide

생성물 1

HCID 57799018Chloromethyl cyclopropyl(4-methyl-3-nitrobenzoyl)carbamate수율 72%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of N-cyclopropyl-4-methyl-3-nitrobenzamide (2.10 g, 9.5 mmol) in THF (48 mL) under nitrogen at −78° C. was added lithium bis(trimethylsilyl)amide (1M, THF, 11.4 mL) over 10 min. After 0.5 h, chloromethyl carbonochloridate (1.1 mL, 12.4 mmol) was added. After 10 min., the cold bath was removed, and the reaction was stirred to room temperature for 1.5 h, quenched with water and concentrated in vacuo. It was then diluted with EtOAc and water. After the layers were separated, the organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. Silica gel chromatography using hexanes:EtOAc (5:1) as eluent afforded the title compound as a colorless oil (2.14 g, 72% yield).

후처리

  1. waitAfter 10 min.
  2. customthe cold bath was removed
  3. customquenched with water
  4. concentrationconcentrated in vacuo
  5. additionIt was then diluted with EtOAc and water
  6. customAfter the layers were separated
  7. dry with materialthe organic layer was dried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-e0ef70a99f6e46048b7a8a363fbde1e9
출처 데이터셋
uspto-grants-2009_08
특허 번호
US07572795B2

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