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Dichloromethane → 2-Chloro-N-cyclopropylmethyl-N-propyl-3-oxo-butanamide

HRID 1057769
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인쇄 미리보기

반응식

HRID 1057769 반응식
[CH:1]1([CH2:4][N:5]([CH2:12][CH2:13][CH3:14])[C:6](=[O:11])[CH2:7][C:8](=[O:10])[CH3:9])[CH2:3][CH2:2]1.S(Cl)([Cl:18])(=O)=O.C(Cl)Cl>C(Cl)(Cl)Cl>[Cl:18][CH:7]([C:8](=[O:10])[CH3:9])[C:6]([N:5]([CH2:4][CH:1]1[CH2:2][CH2:3]1)[CH2:12][CH2:13][CH3:14])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 24648Sulfuryl chlorideHCID 18672242N-Cyclopropylmethyl-N-propyl-3-oxo-butanamide

생성물 1

HCID 186722442-Chloro-N-cyclopropylmethyl-N-propyl-3-oxo-butanamide

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A stirred solution of N-cyclopropylmethyl-N-propyl-3-oxo-butanamide (scheme 2: (H)) (900 mg, 4.57 mmoles) in chloroform (30 mL) at 0° C. was treated with sulfuryl chloride (1M in methylene chloride, 5.48 mL, 5.48 mmoles). The mixture was stirred at room temperature for 30 minutes and then poured into methylene chloride and washed with 5% sodium bicarbonate solution, brine, and dried over Na2SO4. The solution was concentrated in vacuo and the crude product used without further purification.

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후처리

  1. washwashed with 5% sodium bicarbonate solution, brine
  2. dry with materialdried over Na2SO4
  3. concentrationThe solution was concentrated in vacuo
  4. customthe crude product used without further purification

출처 및 근거

ORD 기록
ord-db412722ed2e42db97cb006b4e7bcf09
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06515005B2

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