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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585728Generated: October 26, 2026

Water → 5-Oxo-2,3,4,5-tetrahydro-1-benzothiepine-8-carbonitrile

https://huagongshe.com/reaction/585728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
Reactant8-bromo-3,4-dihydro-2H-benzo[b]thiepin-5-oneHCID 22337456—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
Product5-Oxo-2,3,4,5-tetrahydro-1-benzothiepine-8-carbonitrileHCID 22337418—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 8-bromo-5-oxo-2,3,4,5-tetrahydro-1-benzothiepine (5.00 g) synthesized according to a known method in N,N-dimethylformamide (50 ml) were added zinc cyanide (2.28 g) and tetrakis(triphenylphosphine)palladium(0) (1.13 g) and the mixture was stirred at 80-90° C. for 1 hr. The reaction mixture was allowed to warm to room temperature and water (500 ml) and ethyl acetate (100 ml) were added. The mixture was passed through celite. The filtrate was extracted with ethyl acetate and the organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure and the obtained residue was recrystallized from ethyl acetate and hexane to give the objective 5-oxo-2,3,4,5-tetrahydro-1-benzothiepine-8-carbonitrile (3.37 g) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933305B2
Source datasetuspto-grants-2005_08
ORD IDord-9e07f701113149388ba08da50356ad64
Source noteuspto-grants-2005_08