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4-Chloro-N-(1,1-dimethyl-2-propynyl)benzamide → 2-(4-Chlorophenyl)-4,5-dihydro-4,4-dimethyl-5-methyleneoxazole

HRID 1107059
ノート
印刷プレビュー

反応式

HRID 1107059 の反応式
[CH3:1][C:2]([NH:6][C:7](=[O:15])[C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1)([CH3:5])[C:3]#[CH:4]>[Cu]Cl.C(OCCCC)(=O)C>[Cl:14][C:11]1[CH:12]=[CH:13][C:8]([C:7]2[O:15][C:3](=[CH2:4])[C:2]([CH3:1])([CH3:5])[N:6]=2)=[CH:9][CH:10]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 327384-Chloro-N-(1,1-dimethyl-2-propynyl)benzamide

生成物 1

HCID 108678552-(4-Chlorophenyl)-4,5-dihydro-4,4-dimethyl-5-methyleneoxazole収率 100.2%

試薬・触媒・溶媒 2

HCID 62652Cuprous chloride触媒HCID 31272Butyl Acetate溶媒

反応条件

温度
95 °C

実験手順

A round bottom flask was charged with N-(3-methylbutyn-3-yl)-4-chlorobenzamide (4.5 g, 19.09 mmol), copper(I) chloride (9.5 mg, 0.5 mol %), and n-butyl acetate (20 mL). The resulting mixture was heated to 95° C. for 4 h, then cooled to room temperature. The reaction was washed with 1 M hydrochloric acid solution and with water. The organic layer was dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure, and the residue was dried in a vacuum oven to afford 2-(4-chlorophenyl)-4,4-dimethyl-5-methyleneoxazoline (4.24 g, 94% yield) as a pale yellow oil (bp 95° C., 0.6 mm Hg).

後処理

  1. temperaturecooled to room temperature
  2. washThe reaction was washed with 1 M hydrochloric acid solution and with water
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. customThe solvent was removed by evaporation under reduced pressure
  5. customthe residue was dried in a vacuum oven

出典と根拠

ORDレコード
ord-c58de19889f94a969e34a18c6c4e3933
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06057477

反応ノート

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