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Phosgene → [2-(3-Methyl-1,2,4-oxadiazol-5-yl)phenyl]carbamoyl Chloride

HRID 53241
ノート
印刷プレビュー

反応式

HRID 53241 の反応式
[CH3:1][C:2]1[N:6]=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[NH2:13])[O:4][N:3]=1.[C:14](Cl)([Cl:16])=[O:15]>ClCCl>[CH3:1][C:2]1[N:6]=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[NH:13][C:14]([Cl:16])=[O:15])[O:4][N:3]=1
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 6371PhosgeneHCID 126766822-(3-Methyl-1,2,4-oxadiazol-5-yl)aniline

生成物 1

HCID 19962135[2-(3-Methyl-1,2,4-oxadiazol-5-yl)phenyl]carbamoyl Chloride

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 2-(3-methyl-1,2,4-oxadiazol-5-yl)benzenamine (1.0 g) in dry dichloromethane (20 ml) was added dropwise to a 0° solution of phosgene (14.1 ml, 20% in toluene) in dry dichloromethane (50 ml) under a nitrogen atmosphere. After addition the reaction mixture was allowed to slowly attain room temperature and stirred for 4 h. Nitrogen, was bubbled through the resulting mixture for 16 h. Dichloromethane was added to the resultant precipitate and the solution was evaporated to give the title compound (1.322 g), max (Nujol) 2800-2500, 1782 (NCO-Cl), 1631 (C=N), 1501 (NH), 769 (aromatic) cm-1.

後処理

  1. additionAfter addition the reaction mixture
  2. customwas allowed to slowly attain room temperature
  3. customNitrogen, was bubbled through the resulting mixture for 16 h
  4. additionDichloromethane was added to the resultant precipitate
  5. customthe solution was evaporated

出典と根拠

ORDレコード
ord-3bb9fe0c9a7d418180e0999f8eff48f8
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05618827

反応ノート

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