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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556473Generated: October 25, 2026

Ethyl 6-methoxy-1H-indole-2-carboxylate → Rac-6-methoxy-2,3-dihydro-1h-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/556473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-methoxy-1H-indole-2-carboxylateHCID 612959—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventTrifluoroacetic acidHCID 6422—
ProductRac-6-methoxy-2,3-dihydro-1h-indole-2-carboxylic acid ethyl esterHCID 5747905775.3%

Reaction Steps

Sodium cyanoborohydride (750 mg, 12 mmol) (Aldrich) was added in small portions to a mixture of 6-Methoxy-1H-indole-2-carboxylic acid ethyl ester (500 mg, 2.4 mmol) (Aldrich) in TFA (10 mL), which was cooled in ice-water bath, at such a rate that gas evolution was not too vigorous. When the addition was complete, the mixture was allowed to warm to room temperature and stirred for 2.5 hr. The resulting mixture was concentrated in vacuo and the residue was dissolved in DCM. The organic layer was washed with Na2CO3 solution, dried with Na2SO4, and concentrated to give 400 mg rac-6-Methoxy-2,3-dihydro-1H-indole-2-carboxylic acid ethyl ester. MS: [M+H]+=222

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058269B2
Source datasetuspto-grants-2011_11
ORD IDord-3b507d3ac117459fb37570dde41f7ff5
Source noteuspto-grants-2011_11