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Chlorosuccinimide → Chloro[1-(4-methoxyphenyl)cyclopropyl]acetaldehyde

HRID 500110
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인쇄 미리보기

반응식

HRID 500110 반응식
N1CCC[C@H]1C(O)=O.[CH3:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]2([CH2:20][CH:21]=[O:22])[CH2:19][CH2:18]2)=[CH:13][CH:12]=1.[Cl:23]N1C(=O)CCC1=O>C(Cl)(Cl)Cl>[Cl:23][CH:20]([C:17]1([C:14]2[CH:15]=[CH:16][C:11]([O:10][CH3:9])=[CH:12][CH:13]=2)[CH2:19][CH2:18]1)[CH:21]=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 31398ChlorosuccinimideHCID 145742L-ProlineHCID 86621501[1-(4-Methoxyphenyl)cyclopropyl]acetaldehyde

생성물 1

HCID 86621500Chloro[1-(4-methoxyphenyl)cyclopropyl]acetaldehyde

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

L-Proline (10 mg, 0.1 mmol) was added to a solution of [1-(4-methoxyphenyl)cyclopropyl]acetaldehyde (100 mg, 0.53 mmol) in chloroform (1 mL) at 0° C. followed by addition of N-chlorosuccinimide (84 mg, 0.63 mmol). The reaction mixture was stirred at ambient temperature for 2 h. The mixture was diluted with hexanes and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by flash chromatography eluting with ethyl acetate in hexanes (0-10%) to afford the desired product.

후처리

  1. filtrationfiltered
  2. concentrationThe filtrate was concentrated under reduced pressure
  3. customthe residue was purified by flash chromatography
  4. washeluting with ethyl acetate in hexanes (0-10%)

출처 및 근거

ORD 기록
ord-6339feab97db480994be8e84a3fbe87e
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07767675B2

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