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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293211Generated: November 1, 2026

Methanol → 2-chloro-6,11-dihydro-5H-dibenz[b,e]azepine

https://huagongshe.com/reaction/2293211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantBoron, trihydro(thiobis(methane))-, (T-4)-HCID 9833925—
Reactant2-Chloro-5H-dibenzo[b,e]azepine-6,11-dioneHCID 13466532—
SolventTetrahydrofuranHCID 8028—
Product2-chloro-6,11-dihydro-5H-dibenz[b,e]azepineHCID 5379163864.1%

Reaction Steps

To a mixture of 7.28 g of 2-chloro-5H-dibenz[b,e]azepine-6,11-dione in 25 ml of anhydrous tetrahydrofuran, under argon, is added dropwise 8.5 ml of (10M) boron-dimethyl sulfide. The reaction mixture is stirred at room temperature for 18 hours. The reaction mixture is heated at reflux for 3 hours and cooled to room temperature. While stirring, 25 ml of methyl alcohol is carefully added, followed by 100 ml of 2N NaOH. The reaction mixture is heated at reflux for 24 hours and the solid collected. The solid is dissolved in methylene chloride and washed with 2N citric acid, water and dried (Na2SO4). The volatiles are evaporated in vacuo to give 4.16 g of a residue which is crystallized from ethyl acetate-hexane to give 2.05 g of the desired product as a crystalline solid, m.p. 137°-141° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686445
Source datasetuspto-grants-1997_11
ORD IDord-e31ce4a0c8e24af28ec51566de4bad47
Source noteuspto-grants-1997_11