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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12614Generated: October 30, 2026

Methanol → Methyl 4-bromo-1H-indole-3-carboxylate

https://huagongshe.com/reaction/12614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium CyanideHCID 8929—
Reactant4-Bromo-1H-indole-3-carbaldehydeHCID 2763178—
CatalystHCID 178418406HCID 178418406—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-bromo-1H-indole-3-carboxylateHCID 13499091—

Reaction Steps

To a methanol (40 mL) solution of 4-bromo-1H-indole-3-carboaldehyde [Chem. Pharm. Bull. 33,3696 (1985)] (395 mg), sodium cyanide (432 mg) and manganese dioxide (15.3 g) were sequentially added and the mixture was stirred overnight at room temperature. To the reaction mixture, ethyl acetate (50 mL) was added and insoluble matters were removed. The filtrate was concentrated and water was added to the residue, and then the solution was extracted with ethyl acetate. The organic layer was washed in turn with water and saturated saline, dried and then concentrated. The residue was washed with diisopropyl ether and n-hexane and then concentrated to obtain the titled compound having the following physical properties (375 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728023B2
Source datasetuspto-grants-2010_06
ORD IDord-b898882e96cb45c1803327a8130cdd74
Source noteuspto-grants-2010_06