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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457628Generated: November 2, 2026

5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-one → 10,11-Dihydro-5h-dibenzo[b,e][1,4]diazepine

https://huagongshe.com/reaction/1457628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-oneHCID 201327—
SolventTetrahydrofuranHCID 8028—
Product10,11-Dihydro-5h-dibenzo[b,e][1,4]diazepineHCID 3604679.7%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a stirred solution of 4.3 g of 5,11-dihydro-10H-dibenz[b,e][1,4]diazepin-11-one in 50 ml of tetrahydrofuran, under nitrogen and cooled to 0° C. is added 4.0 ml of a 10 molar solution of dimethyl sulfide-borane complex in tetrahydrofuran. The ice bath is removed after 30 minutes and the reaction mixture stirred at room for 18 hours. The reaction mixture is cooled in an ice bath and 30 ml of anhydrous methanol added dropwise and evaporated to dryness in vacuo. Another 30 ml of methanol is added and evaporated to a residue. The residue is quenched with 30 ml of 40% sodium hydroxide followed by heating at 110° C. for 45 minutes and cooling to room temperature. The reaction mixture is diluted with 200 ml of water and extracted with methylene chloride (3×100 ml). The combined extracts are washed with 1N HCl, water and 0.5N NaOH. The organic layer is dried and evaporated in vacuo to give 3.2 g of the desired product, m.p. 114°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849735
Source datasetuspto-grants-1998_12
ORD IDord-746af68681f5406c804661b58e33e079
Source noteuspto-grants-1998_12