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Methyl chloroacetate → HCID 11629788, 화합물

HRID 703809
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HRID 703809 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7295Methyl chloroacetateHCID 79323-ChloroanilineHCID 516892Sodium Bicarbonate

생성물 1

HCID 11629788HCID 11629788, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-bab85053286144c291524e19bcde6f1c
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04985427

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