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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732137Generated: November 1, 2026

HCID 748083, compound → (3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline

https://huagongshe.com/reaction/1732137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 748083HCID 748083—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carbolineHCID 1337550679.4%

Reaction Steps

A mixture of 15 g of methyl (3S)-1,2,3,4-tetrahydro-β-carboline-3-carboxylate, 6.99 g of NaBH4, and 225 ml of 80% ethanol is stirred at room temperaure for 12 hours, and then refluxed for 1.5 hours. The insoluble materials are filtered off and washed with hot ethanol. The filtrate and the washing are combined and distilled to remove the solvent. Water (40 ml) is added to the residue, and the solution is stirred for 40 minutes. The precipitates are collected by filtration, dried and then recrystallized from ethanol. 9.03 g of (3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-β-carboline are obtained as colorless needles. Yield: 79.4%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04625032
Source datasetuspto-grants-1986_11
ORD IDord-5edd9d6a424244c994f90faa1f2ceb54
Source noteuspto-grants-1986_11