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Water → HCID 20470805, 화합물

HRID 1388296
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HRID 1388296 반응식
[C:1]([NH:4][CH:5]1[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[OH:14])[C:6]1=[O:15])(=[O:3])[CH3:2].[H-].[Na+].[CH3:18][S:19][CH2:20]Cl.O>CN(P(N(C)C)(N(C)C)=O)C>[C:1]([NH:4][CH:5]1[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[O:14][CH2:18][S:19][CH3:20])[C:6]1=[O:15])(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 16916Chloromethyl methyl sulfideHCID 24758Sodium hydrideHCID 20470798N-(4-Hydroxy-1-oxo-2,3-dihydro-1H-inden-2-yl)acetamide

생성물 1

HCID 20470805HCID 20470805, 화합물

시약·촉매·용매 1

HCID 12679Hexamethylphosphoramide용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To 2-acetylamino-4-hydroxy-1-indanone 10.25 g (0.05 m) in 50 ml of dry HMPA under N2 is added 2.6 g (0.055 m) of a 50% oil dispersion of sodium hydride in portions. After stirring at room temperature for 1/2 hr, 5.3 g (0.055 m) of chloromethyl methyl sulfide is added, and the mixture is stirred overnight. Water is added and the mixture is extracted with ethyl acetate which is back-washed with water. After drying (Na2SO4) and concentration, the desired product is obtained.

후처리

  1. stirringthe mixture is stirred overnight
  2. extractionthe mixture is extracted with ethyl acetate which
  3. washis back-washed with water
  4. customAfter drying
  5. concentration(Na2SO4) and concentration

출처 및 근거

ORD 기록
ord-21ab3372c1144164aa28c71bf92e7848
출처 데이터셋
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04431647

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