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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801704Generated: October 31, 2026

Water → 3-Hydroxymethyl-beta-carboline

https://huagongshe.com/reaction/1801704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl 9H-pyrido(3,4-b)indole-3-carboxylateHCID 107704—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product3-Hydroxymethyl-beta-carbolineHCID 535333884.1%

Reaction Steps

3.5 grams (15 mmol) of 3-carbomethoxy-β-carboline were suspended in 300 ml THF, 2.7 grams (75 mmol) sodium borohydride were added and the mixture was stirred at room temperature for 12 hours. The mixture was then cooled, 50 ml water were added and the resulting mixture was stirred overnight. The solvent was evaporated under reduced pressure and water (300 ml) was again added. The aqueous suspension was extracted with dichloromethane, followed by ethylacetate, the organic extracts were combined, and the solvent was evaporated under reduced pressure. The remaining residue was purified by column chromatography on silica gel, using and a 9:1 mixture of ethylacetate and methanol as eluent, to give 3-(hydroxymethyl)-β-carboline (2.5 grams, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349850B2
Source datasetuspto-grants-2013_01
ORD IDord-a75f5ece28d046178dc1d6e4ed2d2fb2
Source noteuspto-grants-2013_01