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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855313Generated: October 26, 2026

Ethanol → 3-(Methylamino)-1-(thiophen-2-yl)propan-1-ol

https://huagongshe.com/reaction/1855313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantSodiumHCID 5360545—
Reactant1-Propanone, 3-(methylamino)-1-(2-thienyl)-, hydrochloride (1:1)HCID 10035872—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product3-(Methylamino)-1-(thiophen-2-yl)propan-1-olHCID 1021442084%

Reaction Steps

To a mixture of 3-(methylamino)-1-(thiophen-2-yl)propan-1-one hydrochloride (10.3 g, 50 mmol) and ethanol (35 mL) at 4° C. sodium hydroxide (4.0 g of a 50% aqueous solution) was added in about 5 minutes. Afterwards, neat sodium borhydride (0.95 g, 25 mmol, 1.0 eq) was added in several portions in about 30 minutes. At the end of the addition, the suspension was stirred for 4 h at the same temperature, then acetone (10.0 mL) was added dropwise in 5 minutes and the mixture was stirred for 10 additional minutes. Water (20 mL) was then added. Afterwards, the mixture was concentrated about 5 times under vacuum and the residue was extracted with tert-butyl methyl ether (2×20 mL). The collected organic phases were finally concentrated under vacuum affording an orange oil which crystallised spontaneously after a few hours. Finally, an orange solid was obtained (7.2 g, 84% yield). This compound can then be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962865B2
Source datasetuspto-grants-2015_02
ORD IDord-c63b9b3d476b45ee865ffea31bebf3e0
Source noteuspto-grants-2015_02