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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255948Generated: November 2, 2026

Methanol → 5,6,7,8-Tetrahydro-4H-thieno[3,2-B]azepine

https://huagongshe.com/reaction/2255948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4H,5H,6H,7H,8H-thieno[3,2-b]azepin-5-oneHCID 870743—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
SolventTetrahydrofuranHCID 8028—
Product5,6,7,8-Tetrahydro-4H-thieno[3,2-B]azepineHCID 1180497179.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 21.2 g of 5,6,7,8-tetrahydro-4H-thieno[3 2-b]azepin-5-one in 100 ml of tetrahydrofuran under argon, chilled to 0° C. is added 25.2 ml of a 10.0 molar solution of borane-dimethylsulfide in tetrahydrofuran. The solution is stirred at room temperature for 16 hours and is refluxed for 5 hours. The mixture is cooled to room temperature and 85 ml of methanol added dropwise (exotherm). The solvent is removed and 100 ml of methanol is added (2 times) and after each addition the solvent is removed. To the residual solid (dried under vacuum) is added 126 ml of 2N NaOH and the mixture refluxed 3 hours. The mixture is chilled (2 hours) and extracted with dichloromethane. The extract is dried (Na2SO4) and the solvent removed to give 15.4 g of brown solid, m.p. 55°-57° C. A sample (3 g) is sublimed to give 2.6 g of crystals, m.p. 64°-65° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654297
Source datasetuspto-grants-1997_08
ORD IDord-151df3ab53da414e96e3983949baa404
Source noteuspto-grants-1997_08