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Methyl chloroacetate → HCID 11629788、化合物

HRID 703809
ノート
印刷プレビュー

反応式

HRID 703809 の反応式
C(=O)(O)[O-].[Na+].[Cl:6][C:7]1[CH:8]=[C:9]([CH:11]=[CH:12][CH:13]=1)[NH2:10].Cl[CH2:15][C:16]([O:18][CH3:19])=[O:17]>CCOCC>[CH3:19][O:18][C:16](=[O:17])[CH2:15][NH:10][C:9]1[CH:11]=[CH:12][CH:13]=[C:7]([Cl:6])[CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7295Methyl chloroacetateHCID 79323-ChloroanilineHCID 516892Sodium Bicarbonate

生成物 1

HCID 11629788HCID 11629788、化合物

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

A mixture of sodium bicarbonate (66 g), 3-chloroaniline (50 g) and methyl chloroacetate (51.5 ml) were stirred under nitrogen at 80°-100° for 6 h. Heating at 90° was continued overnight, and the mixture was then cooled and poured into ether (400 ml). The resultant suspension was stirred, chilled to 0°, the precipitated solid was filtered off and the filtrate was retained. The solid was dissolved in ethyl acetate (400 ml) and washed with water (2×200 ml), followed by dilute hydrochloric acid (200 ml). The organic phase was dried and concentrated in vacuo to give the title compound (16.4 g) as a solid, m.p. 75°-76°. The previously obtained filtrate was washed with dilute hydrochloric acid (200 ml), and the organic phase was separated, dried and concentrated in vacuo to give an oily solid. This was triturated with ether:hexane (1:1; 300 ml) and filtered off to give a further batch of the title compound (20 g).

後処理

  1. temperatureHeating at 90°
  2. waitwas continued overnight
  3. temperaturethe mixture was then cooled
  4. temperaturechilled to 0°
  5. filtrationthe precipitated solid was filtered off
  6. dissolutionThe solid was dissolved in ethyl acetate (400 ml)
  7. washwashed with water (2×200 ml)
  8. customThe organic phase was dried
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-bab85053286144c291524e19bcde6f1c
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04985427

反応ノート

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