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Chloroacetyl chloride → 2-chloro-N-(4-fluorobenzyl)acetamide

HRID 2120934
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HRID 2120934 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH2:7])=[CH:4][CH:3]=1.C(N(CC)CC)C.[Cl:17][CH2:18][C:19](Cl)=[O:20]>O1CCCC1>[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH:7][C:19](=[O:20])[CH2:18][Cl:17])=[CH:4][CH:3]=1
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참가 물질

5

반응물 3

HCID 6577Chloroacetyl chlorideHCID 8471TriethylamineHCID 673264-Fluorobenzylamine

생성물 1

HCID 23037092-chloro-N-(4-fluorobenzyl)acetamide수율 91%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred mixture of 4-fluorobenzylamine (685 uL, 6.0 mmol) and dry tetrahydrofuran (20 mL) was added triethylamine (1.25 mL, 9.0 mmol) under nitrogen. The resulting mixture was stirred for 10 minutes at ambient temperature. Next, chloroacetyl chloride (477 uL, 6.0 mmol) was added and the resulting mixture was stirred for 1 h. at ambient temperature. The resulting mixture was partitioned between ethyl acetate and water. The organic layer was washed with water (2×20 mL) and brine (1×20 mL), dried over magnesium sulfate, and filtered. Evaporation of the filtrate in vacuo followed by chromatography on silica gel eluting with ethyl acetate-hexane gave 1.09 g (91%) of the pure title compound.

후처리

  1. stirringthe resulting mixture was stirred for 1 h. at ambient temperature
  2. customThe resulting mixture was partitioned between ethyl acetate and water
  3. washThe organic layer was washed with water (2×20 mL) and brine (1×20 mL)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customEvaporation of the filtrate in vacuo

출처 및 근거

ORD 기록
ord-dd32ef2172d64608bb7c5d6fc8e48da0
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06693137B1

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