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Ammonium Hydroxide → (E)-2-(6-fluoro-1-indanylidene)acetamide

HRID 862762
ノート
印刷プレビュー

反応式

HRID 862762 の反応式
[OH-].[NH4+:2].[F:3][C:4]1[CH:12]=[C:11]2[C:7]([CH2:8][CH2:9]/[C:10]/2=[CH:13]\[C:14](Cl)=[O:15])=[CH:6][CH:5]=1>ClCCl>[F:3][C:4]1[CH:12]=[C:11]2[C:7]([CH2:8][CH2:9]/[C:10]/2=[CH:13]\[C:14]([NH2:2])=[O:15])=[CH:6][CH:5]=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 14923Ammonium HydroxideHCID 15491026(E)-2-(6-fluoro-1-indanylidene)acetyl chloride

生成物 1

HCID 9837001(E)-2-(6-fluoro-1-indanylidene)acetamide収率 91%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A 29.6% aqueous ammonium hydroxide solution (17.6 mL, 134 mmol) was added dropwise to a stirred, chilled (ice bath) solution of (E)-2-(6-fluoro-1-indanylidene)acetyl chloride (14.1 g, 67 mmol) in dichloromethane (165 mL). After an hour, the resulting white precipitate was collected by filtration, dissolved in ethyl acetate (600 mL) and washed with water (3×300 mL). The ethyl acetate layer was dried over sodium sulfate and concentrated in vacuo. The resulting off-white solid was washed with hexane, giving 11.6 g (91%) of (E)-2-(6-fluoro-1-indanylidene)acetamide, m.p., 180°-183° C.; NMR (DMSO-d6): d6.91-7.41 (m, 5H, Ar+NH2), 6.37 (t,1H, =CH), 2.92-2.96, 3.16-3.22 (2m's, 4H, 2XCH2); steady-state nOe:irradiation at 6.37 d, observed 23% nOe at 7.28 d.

後処理

  1. waitAfter an hour
  2. filtrationthe resulting white precipitate was collected by filtration
  3. dissolutiondissolved in ethyl acetate (600 mL)
  4. washwashed with water (3×300 mL)
  5. dry with materialThe ethyl acetate layer was dried over sodium sulfate
  6. concentrationconcentrated in vacuo
  7. washThe resulting off-white solid was washed with hexane

出典と根拠

ORDレコード
ord-6b25dcb32f2b4c7f959757bea9405c7d
出典データセット
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05719186

反応ノート

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