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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376207Generated: October 25, 2026

Water → 3-(N-Methylamino)-1-(2-thienyl)-1-propanol, (-)-

https://huagongshe.com/reaction/1376207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant(βS)-β-Hydroxy-N-methyl-2-thiophenepropanamideHCID 10261821—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product3-(N-Methylamino)-1-(2-thienyl)-1-propanol, (-)-HCID 1009504795.1%

Reaction Steps

1728 ml of dry tetrahydrofuran are initially charged with 52 g of lithium aluminium hydride and heated to reflux. At the same time, dropwise addition of 86.4 g of N-methyl-(3S)-3-hydroxy-3-(2-thienyl)propanamide dissolved in 692 g of tetrahydrofuran is commenced. Once dropwise addition is complete, stirring is continued under reflux overnight. The reaction mixture is then cooled to room temperature and 1037 ml of water are cautiously added dropwise. 173 ml of a 10% sodium hydroxide solution were then added dropwise and the solution was filtered. The solvent was removed under reduced pressure. The crude solution was admixed with 346 ml of 1 N sodium hydroxide solution and extracted 3 times with 345 ml of toluene each time. The organic phases are combined and the volatile constituents are removed under reduced pressure to obtain 76 g of (1S)-3-(methylamino)-1-(2-thienyl)-1-propanol (84% purity, 80% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169938B2
Source datasetuspto-grants-2007_01
ORD IDord-ead2dfa318114c3daba0c8209e705a63
Source noteuspto-grants-2007_01