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Pyridine → 4-Ethyl-2-fluoro-N-(2-hydroxyphenyl)benzamide

HRID 268496
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HRID 268496 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].N1C=CC=CC=1.[CH2:15]([C:17]1[CH:25]=[CH:24][C:20]([C:21](Cl)=[O:22])=[C:19]([F:26])[CH:18]=1)[CH3:16]>C1C=CC=CC=1>[CH2:15]([C:17]1[CH:25]=[CH:24][C:20]([C:21]([NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[OH:8])=[O:22])=[C:19]([F:26])[CH:18]=1)[CH3:16]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 58012-AminophenolHCID 214138374-Ethyl-2-fluorobenzoyl chloride

생성물 1

HCID 214138074-Ethyl-2-fluoro-N-(2-hydroxyphenyl)benzamide

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

To a solution of 13.08 gm. of o-aminophenol in 150 cc. of dry pyridine which is cooled in ice water is added a solution of 4-ethyl-2-fluorobenzoyl chloride (prepared from 20.0 gm. of acid and thionyl chloride) in 30 cc. of dry benzene. The mixture is stirred at room temperature overnight and then concentrated in vacuo. The residue is treated with water and the precipitate collected by filtration to give crude 4-ethyl-2-fluoro-2'-hydroxybenzanilide which was characterized by infra red spectra then used in the following step.

후처리

  1. concentrationconcentrated in vacuo
  2. additionThe residue is treated with water
  3. filtrationthe precipitate collected by filtration

출처 및 근거

ORD 기록
ord-a5b5cc4344694a73aff36ec7f2caacf3
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03947582

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