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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457621Generated: October 30, 2026

Methanol → 9Chloro-6,11-dihydro-5H-dibenz[b,e]azepine

https://huagongshe.com/reaction/1457621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron, trihydro(thiobis(methane))-, (T-4)-HCID 9833925—
Reactant9-Chloro-5H-dibenz[b,e]azepin-6,11-dioneHCID 54011703—
SolventTetrahydrofuranHCID 8028—
Product9Chloro-6,11-dihydro-5H-dibenz[b,e]azepineHCID 5417492864.7%

Reaction Steps

To a mixture of 7.28 g 9-chloro-5H-dibenz-[b,e]azepin-6,11-dione in 25 ml of tetrahydrofuran under argon is added 8.5 ml of 10 molar boron-dimethylsulfide in tetrahydrofuran. The mixture is stirred 18 hours at room temperature, 30 ml of tetrahydrofuran added and the mixture refluxed for 3 hours (solids dissolved). The solution is cooled to room temperature and 25 ml of methanol added dropwise. The volatiles are removed under vacuum. To the residue is added 100 ml of 2N NaOH. The mixture is refluxed overnight and filtered. The solid is extracted with dichloromethane and the extract is washed with 2N citric acid, water and dried (Na2SO4). The solvent is removed to give 4.2 g of solid which is triturated with ethyl acetate-hexane (1:2) to give crystals, m.p. 137° C. to 141° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849735
Source datasetuspto-grants-1998_12
ORD IDord-36ed59aa81c14f2a9604ff13b4c5b93f
Source noteuspto-grants-1998_12