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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355840Generated: October 25, 2026

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

https://huagongshe.com/reaction/355840

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 of 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 numberUS05834461
Source datasetuspto-grants-1998_11
ORD IDord-1260298fdc824566b8f70165337297f2
Source noteuspto-grants-1998_11