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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915006Generated: October 31, 2026

Tetrahydrofuran → 3-Hydroxymethyl-beta-carboline

https://huagongshe.com/reaction/1915006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 9H-pyrido(3,4-b)indole-3-carboxylateHCID 107704—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Product3-Hydroxymethyl-beta-carbolineHCID 5353338—

Reaction Steps

3-carbomethoxy-β-carboline or a derivative thereof (J in Scheme VII above) is dissolved in a polar solvent (e.g., THF), and a reducing agent (e.g., NaBH4) is added to the solution. The mixture is stirred for a few hours and cooled. An excess of water is then added, and the mixture is stirred for another few hours. The solvent is thereafter evaporated and the resulting residue is dissolved in water, washed several times with one or more non-polar solvents such as dichloromethane and ethyl acetate, and the combined organic extracts are then evaporated. The remaining residue is purified by column chromatography (e.g., on a silica gel with elution by a 9:1 mixture of ethylacetate and methanol), to give a 3-hydroxymethyl-β-carboline intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614319B2
Source datasetuspto-grants-2013_12
ORD IDord-2586272a565f4c7dbbf0cc94a4fed88c
Source noteuspto-grants-2013_12