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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903647Generated: October 31, 2026

Water → 2-Trifluoromethyl-9-chloro-10,11-dihydrodibenzo[b,f]thiepin

https://huagongshe.com/reaction/903647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Trifluoromethyl-9-chloro-11-chloro-10,11-dihydrodibenzo[b,f]thiepinHCID 12687118—
ReactantAluminate (Al(OH)41-), lithium, (T-4)-HCID 16206110—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-Trifluoromethyl-9-chloro-10,11-dihydrodibenzo[b,f]thiepinHCID 1268712018%

Reaction Steps

To the mixture of 0.2 g of lithium aluminum hydride and 20 ml of anhydrous tetrahydrofuran was added with stirring under ice-cooling 400 mg of 2-trifluoromethyl-9-chloro-11-chloro-10,11-dihydrodibenzo[b,f]thiepin dissolved in 10 ml of anhydrous tetrahydrofuran. Thereafter, the mixture was reacted under cooling for 0.5 hr. at the room temperature and further under reflux condition for 3.5 hrs. After cooling, to the mixture was added water with stirring under cooling to decompose an excess of lithium aluminum hydroxide and the resulting mixture was filtered with the use of celite. The filtrate was extracted with chloroform, chloroform layer was washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain 372 ml of an oily substance, which was chromatographed on a silica gel, eluted with n-hexane, and there was obtained 65 mg of 2-trifluoromethyl-9-chloro-10,11-dihydrodibenzo[b,f]thiepin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04228284
Source datasetuspto-grants-1980_10
ORD IDord-71c31ba5e0764dd3adf1c7afae887897
Source noteuspto-grants-1980_10