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Ethyl bromoacetate → Ethyl 2-[4-(2-bromoethyl)-3-chlorophenoxy]acetate

HRID 2185025
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반응식

HRID 2185025 반응식
[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][C:5]=1[Cl:11].C(=O)([O-])[O-].[K+].[K+].Br[CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21]>CC(C)=O>[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])=[CH:6][C:5]=1[Cl:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 224594084-(2-Bromoethyl)-3-chlorophenol

생성물 1

HCID 12049887Ethyl 2-[4-(2-bromoethyl)-3-chlorophenoxy]acetate

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a stirred solution of 4-(2-bromoethyl)-3-chlorophenol (158 mg) in acetone (7 ml) were added potassium carbonate (139 mg) and ethyl bromoacetate (89 μl) at room temperature. After the mixture was stirred for 20 hours at room temperature, the insoluble material was filtered off and the filtrate was concentrated in vacuo. Purification of the residue by medium pressure liquid column chromatography on silica gel (eluent: hexane/ethyl acetate 7/1) gave ethyl 2-[4-(2-bromoethyl)-3-chlorophenoxy]acetate (193 mg).

후처리

  1. filtrationthe insoluble material was filtered off
  2. concentrationthe filtrate was concentrated in vacuo
  3. customPurification of the residue by medium pressure liquid column chromatography on silica gel (eluent: hexane/ethyl acetate 7/1)

출처 및 근거

ORD 기록
ord-2f99117a4a784d0b802a708cedd321aa
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06399660B1

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