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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574129Generated: October 25, 2026

Water → 3-Hydroxymethyl-beta-carboline

https://huagongshe.com/reaction/574129

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 was 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 numberUS09034872B2
Source datasetuspto-grants-2015_05
ORD IDord-c666e84aa64b4cfc94e963aa8033cbac
Source noteuspto-grants-2015_05