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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887203Generated: October 29, 2026

Sodium cyanoborohydride → 6-Bromo-2,3-dihydro-5-methyl-1H-indole

https://huagongshe.com/reaction/1887203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-bromo-5-methyl-1H-indoleHCID 10750926—
SolventAcetic AcidHCID 176—
Product6-Bromo-2,3-dihydro-5-methyl-1H-indoleHCID 1894091871.1%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of 6-bromo-5-methylindole (1.00 g, 4.75 mmol) in AcOH (150 mL) was treated with NaBH3CN (0.897 g, 14.3 mmol) while maintaining a temperature of −10° C. The mixture was then stirred at RT overnight and concentrated. The resulting residue was treated with aqueous K2CO3, and extracted with DCM (3×100 mL). The combined organic layers were dried over MgSO4, concentrated and purified by column chromatography (0-75% EtOAc/hexanes) to afford 6-bromo-5-methylindoline (13A, 716 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501747B2
Source datasetuspto-grants-2013_08
ORD IDord-828da0fa6ef946e282415e803e7bdf80
Source noteuspto-grants-2013_08