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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732133Generated: November 1, 2026

Ethanol → HCID 13653084, compound

https://huagongshe.com/reaction/1732133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13653070HCID 13653070—
SolventWaterHCID 962—
ProductHCID 13653084HCID 1365308465%

Reaction Steps

A mixture of 0.577 g of methyl (3S)-6-fluoro-1,2,3,4-tetrahydro-β-carboline-3-carboxylate hydrochloride, 0.32 g of sodium borohydride, 20 ml of ethanol and 10 ml of water is stirred at room temperature for 21 hours, and then further refluxed for 3 hours. After the reaction, insoluble materials are removed by filtration and washed with hot ethanol. The filtrate and washings are combined and concentrated. Water is added to the residue, and crystalline precipitates are collected by filtration and dried, whereby 286 mg of (3S)-3-hydroxymethyl-6-fluoro-1,2,3,4-tetrahydro-β-carboline are obtained as colorless needles. Yield: 65%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04625032
Source datasetuspto-grants-1986_11
ORD IDord-7b3db535d3554275906d83bb3facd803
Source noteuspto-grants-1986_11