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4-Fluorobenzoyl chloride → N-(3-Cyano-4,5-dihydro-2-furanyl)-4-fluorobenzamide

HRID 714776
ノート
印刷プレビュー

反応式

HRID 714776 の反応式
[NH2:1][C:2]1[O:3][CH2:4][CH2:5][C:6]=1[C:7]#[N:8].[F:9][C:10]1[CH:18]=[CH:17][C:13]([C:14](Cl)=[O:15])=[CH:12][CH:11]=1>N1C=CC=CC=1>[C:7]([C:6]1[CH2:5][CH2:4][O:3][C:2]=1[NH:1][C:14](=[O:15])[C:13]1[CH:17]=[CH:18][C:10]([F:9])=[CH:11][CH:12]=1)#[N:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 678794-Fluorobenzoyl chlorideHCID 134169562-Amino-4,5-dihydrofuran-3-carbonitrile

生成物 1

HCID 7655792N-(3-Cyano-4,5-dihydro-2-furanyl)-4-fluorobenzamide収率 96.2%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

To a solution of 2-amino-4,5-dihydrofuran-3-carbonitrile (3.5 g) obtained in Step D in pyridine (8 mL) was added dropwise 4-fluorobenzoyl chloride (5.5 g) in an ice bath, and the mixture was stirred at room temperature for 3 hr. The solvent was evaporated under reduced pressure, and to the residue was added dropwise saturated aqueous sodium hydrogen carbonate solution in an ice bath. The resulting solid was collected by filtration, and washed with water to give the title compound (7.1 g).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe solvent was evaporated under reduced pressure
  2. additionto the residue was added dropwise saturated aqueous sodium hydrogen carbonate solution in an ice bath
  3. filtrationThe resulting solid was collected by filtration
  4. washwashed with water

出典と根拠

ORDレコード
ord-a73523436d094cb5be35d0ab2d8526b0
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187453B2

反応ノート

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