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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373553Generated: October 26, 2026

Potassium Hydroxide → 8-Bromo-2,3,4,5-tetrahydro-1-benzothiepine

https://huagongshe.com/reaction/373553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant8-bromo-3,4-dihydro-2H-benzo[b]thiepin-5-oneHCID 22337456—
SolventDiethylene GlycolHCID 8117—
Product8-Bromo-2,3,4,5-tetrahydro-1-benzothiepineHCID 1993540472.5%

Reaction Steps

15.6 g of 8-bromo-3,4-dihydro-1-benzothiepin-5(2H)-one were dissolved in 70 ml of diethylene glycol. The solution was treated with 6.55 ml of hydrazine hydrate and 7.5 g of solid potassium hydroxide and heated to 180°-190° C. under reflux for about 30 hours. After cooling, the mixture was poured on to ice and extracted with ether. The organic phase was washed with water, dried and evaporated. Chromatography on silica gel with petroleum ether yielded 10.7 g of 8-bromo-2,3,4,5-tetrahydro-1-benzothiepine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05164387
Source datasetuspto-grants-1992_11
ORD IDord-b0f0703c78ac43d8b3aba03979754c12
Source noteuspto-grants-1992_11