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Ethyl chloroacetate → HCID 53739137, 화합물

HRID 1903744
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HRID 1903744 반응식
[O:1]=[C:2]1[CH2:10][C:9]2[C:4](=[CH:5][C:6]([Cl:12])=[C:7]([NH2:11])[CH:8]=2)[NH:3]1.C(=O)([O-])[O-].[K+].[K+].Cl[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22]>CC(C)=O>[O:1]=[C:2]1[CH2:10][C:9]2[C:4](=[CH:5][C:6]([Cl:12])=[C:7]([NH2:11])[CH:8]=2)[N:3]1[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7751Ethyl chloroacetateHCID 11430Potassium CarbonateHCID 204666645-amino-6-chloro-2,3-dihydro-1H-indol-2-one

생성물 1

HCID 53739137HCID 53739137, 화합물수율 19.1%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a mixture of 2-oxo-5-amino-6-chloroindoline (3.2 g), potassium carbonate (4.8 g) and acetone (60 ml) was added dropwise ethyl chloroacetate (3.2 g) at ambient temperature. The reaction mixture was refluxed with stirring for 4 hours and then filtered under warm condition. The filter cake was washed with acetone. The combined filtrate and washings were concentrated under reduced pressure to give a residue, which was purified by a column chromatography on silica gel to give crystalline ethyl 2-oxo-5-amino-6-chloro-1-indolineacetate (0.9 g).

후처리

  1. temperatureThe reaction mixture was refluxed
  2. filtrationfiltered
  3. temperatureunder warm condition
  4. washThe filter cake was washed with acetone
  5. concentrationThe combined filtrate and washings were concentrated under reduced pressure
  6. customto give a residue, which
  7. customwas purified by a column chromatography on silica gel

출처 및 근거

ORD 기록
ord-7c4c5896d65e4cb1ab4c94b61e93c60d
출처 데이터셋
uspto-grants-1984_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04438126

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