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Cesium carbonate → Methyl 2-[2-chloro-3-(hydroxymethyl)phenoxy]acetate

HRID 1250092
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HRID 1250092 반응식
C(=O)([O-])[O-].[Cs+].[Cs+].[Cl:7][C:8]1[C:13]([CH2:14][OH:15])=[CH:12][CH:11]=[CH:10][C:9]=1[OH:16].Br[CH2:18][C:19]([O:21][CH3:22])=[O:20]>CC(C)=O>[CH3:22][O:21][C:19](=[O:20])[CH2:18][O:16][C:9]1[CH:10]=[CH:11][CH:12]=[C:13]([CH2:14][OH:15])[C:8]=1[Cl:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10796Cesium carbonateHCID 60984Methyl bromoacetateHCID 155506102-Chloro-3-(hydroxymethyl)phenol

생성물 1

HCID 15550611Methyl 2-[2-chloro-3-(hydroxymethyl)phenoxy]acetate수율 84.1%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Cesium carbonate (3.42 g, 10.5 mmol) was added to a solution of 2-chloro-3-hydroxymethylphenol (1.59 g, 10 mmol) in acetone at room temperature, and the reaction mixture allowed to stir for 30 minutes. Methyl bromoacetate (1.68 g, 11 mmol) was then added. The mixture was stirred overnight, filtered, and the filtrate was concentrated in vacuo. Purification of the residue by silica gel flash chromatography, eluting with dichloromethane/methanol, gave (2-chloro-3-hydroxymethylphenoxy)acetic acid methyl ester as a white crystalline solid (1.94 g, 84.1%).

후처리

  1. stirringThe mixture was stirred overnight
  2. filtrationfiltered
  3. concentrationthe filtrate was concentrated in vacuo
  4. customPurification of the residue by silica gel flash chromatography
  5. washeluting with dichloromethane/methanol

출처 및 근거

ORD 기록
ord-d40e21d17c7846aab042d412fd4c3b10
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06335459B1

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