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Ammonium Carbonate → 2-(2-Iodophenyl)acetamide

HRID 1778951
ノート
印刷プレビュー

反応式

HRID 1778951 の反応式
[I:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=O.C(=O)([O-])[O-].[NH4+:16].[NH4+]>S(Cl)(Cl)=O>[I:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([NH2:16])=[O:11]
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 2

HCID 517111Ammonium CarbonateHCID 27800902-Iodophenylacetic acid

生成物 1

HCID 184740882-(2-Iodophenyl)acetamide

試薬・触媒・溶媒 1

HCID 24386Thionyl Chloride溶媒

反応条件

温度
60 °C

実験手順

A solution of 2-iodophenylacetic acid (20.5 g, 78.2 mmol) in thionyl chloride (70 mL) was stirred at 75° C. for 3 hours. The thionyl chloride was removed in vacuo and the resulting residue was dissolved in DCM (100 mL). Ammonium carbonate (15.03 g, 156.5 mmol) was added and the resulting mixture was stirred at 60° C. for 20 hours. The volatiles were evaporated in vacuo, water (100 mL) was added and the resulting suspension was sonicated for 1 minute, before filtering and washing the filter cake with water then Et2O. After air drying, the title compound I6 was obtained as a light cream coloured solid (12.9 g, 63%); 1H NMR (300 MHz, d6-DMSO) δ 7.82 (d, J=8.3 Hz, 1H), 7.41 (brs s, 1H), 7.30-7.37 (m, 2H), 6.95-7.01 (m, 2H), 3.55 (s, 2H). LCMS-B: rt 5.108 min; m/z 262 [M+H]+.

後処理

  1. customThe thionyl chloride was removed in vacuo
  2. dissolutionthe resulting residue was dissolved in DCM (100 mL)
  3. customThe volatiles were evaporated in vacuo, water (100 mL)
  4. additionwas added
  5. customthe resulting suspension was sonicated for 1 minute
  6. filtrationbefore filtering
  7. washwashing the filter cake with water
  8. customAfter air drying

出典と根拠

ORDレコード
ord-c5fa446c69f6416cac348e2f004e729e
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09266864B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート