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Dichloromethane → Methyl 5-bromoindoline-7-carboxylate

HRID 387244
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HRID 387244 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:11]([O:13][CH3:14])=[O:12])[CH:10]=1)[N:7](C(OC(C)(C)C)=O)[CH2:6][CH2:5]2.ClCCl.[OH-].[Na+]>FC(F)(F)C(O)=O>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:11]([O:13][CH3:14])=[O:12])[CH:10]=1)[NH:7][CH2:6][CH2:5]2
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참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 14798Sodium HydroxideHCID 497588561-Tert-butyl 7-methyl 5-bromoindoline-1,7-dicarboxylate

생성물 1

HCID 49758858Methyl 5-bromoindoline-7-carboxylate수율 101.5%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

1-(1,1-dimethylethyl) 7-methyl 5-bromo-2,3-dihydro-1H-indole-1,7-dicarboxylate (9 g, 25 mmol) was dissolved in trifluoroacetic acid (6 mL) and stirred at room temperature for 16 hours. Dichloromethane and sodium hydroxide solution (2 M) were added and the organic layer washed twice with sodium hydroxide solution until the aqueous layer pH>7. The organic layer was then concentrated in vacuo to give 6.5 g (100%) of the title compound as a brown solid.

후처리

  1. washthe organic layer washed twice with sodium hydroxide solution until the aqueous layer pH>7
  2. concentrationThe organic layer was then concentrated in vacuo

출처 및 근거

ORD 기록
ord-5c40a508bb024e18afe4c58b76281c2c
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08372875B2

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