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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172990Generated: November 1, 2026

5-Chloro-2-methylindole → 5-chloro-2-methyl-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/1172990

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-methylindoleHCID 70636—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product5-chloro-2-methyl-2,3-dihydro-1H-indoleHCID 59556818100%

Reaction Steps

To a solution of 5-chloro-2-methylindole (1.00 g, 6.04 mmol) in acetic acid (7 ml) was added portionwise sodium cyanoborohydride (0.76 g, 12.1 mmol) and the reaction mixture was stirred at room temperature for 16 hours. The resulting solution was diluted with ethyl acetate and washed sequentially with water and with 5 N aq. sodium hydroxide solution. The organic phase was dried over sodium sulphate and concentrated in vacuo. The residue was purified by chromatography on silica gel (eluant: heptane/ethyl acetate gradient) to yield the title compound as a colourless oil (1.00 g, 100%); MS (ISP): 170.2 ([{37Cl}M+H]+), 168.3 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834044B2
Source datasetuspto-grants-2010_11
ORD IDord-3b885b7d0ce04970b0b4ef443d4d6706
Source noteuspto-grants-2010_11