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ethyl 2-(1-methyl-6,7-dihydro-1H-indol-4(5H)-ylidene)acetate → ethyl 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)acetate

HRID 447746
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HRID 447746 반응식
[CH3:1][N:2]1[C:10]2[CH2:9][CH2:8][CH2:7][C:6](=[CH:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:5]=2[CH:4]=[CH:3]1>[Pd].CCO>[CH3:1][N:2]1[C:10]2[CH2:9][CH2:8][CH2:7][CH:6]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:5]=2[CH:4]=[CH:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 69074859ethyl 2-(1-methyl-6,7-dihydro-1H-indol-4(5H)-ylidene)acetate

생성물 1

HCID 20761741ethyl 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)acetate수율 99.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

Pd—C (1.3 g, 5%) is added to a solution of a mixture of E/Z isomers of ethyl 2-(1-methyl-6,7-dihydro-1H-indol-4(5H)-ylidene)acetate (3.4 g, 15.50 mmoles) in 100 mL de EtOH, and the resulting solution is stirred under hydrogen atmosphere (25 psi) in a Parr hydrogenator for 8 hours. The reaction mixture is purged with nitrogen, filtered through Celite and the solvent is evaporated under reduced pressure to obtain ethyl 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)acetate (3.4 g, 15.36 mmol, 99%, oil).

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후처리

  1. customThe reaction mixture is purged with nitrogen
  2. filtrationfiltered through Celite
  3. customthe solvent is evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-611f8ae3c2ae462d852a598c16dbe7ff
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481567B2

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