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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562007Generated: October 29, 2026

N-bromobutanimide → 1-Tert-butyl 7-methyl 5-bromoindoline-1,7-dicarboxylate

https://huagongshe.com/reaction/562007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-Tert-butyl 7-methyl indoline-1,7-dicarboxylateHCID 49758857—
SolventDichloromethaneHCID 6344—
Product1-Tert-butyl 7-methyl 5-bromoindoline-1,7-dicarboxylateHCID 4975885689%

Reaction Steps

1-(1,1-dimethylethyl) 7-methyl 2,3-dihydro-1H-indole-1,7-dicarboxylate (3.1 g, 11.2 mmol) and N-bromosuccinimide (2.0 g, 11.2 mmol) were dissolved in dry dichloromethane (100 mL) and stirred under a nitrogen atmosphere at room temperature for 16 hours. The reaction was partitioned with sodium hydroxide solution (2 M), separated and washed with more sodium hydroxide solution. The organic layer was dried over magnesium sulfate and concentrated in vacuo to give the title compound as a gummy red solid (3.55 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063071B2
Source datasetuspto-grants-2011_11
ORD IDord-630d134d786c4515b9e3e7eb258db42f
Source noteuspto-grants-2011_11