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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886825Generated: October 26, 2026

Methanol → 4-Benzyl-8-bromo-2,3,4,5-tetrahydrobenzo[f][1,4]oxazepine

https://huagongshe.com/reaction/886825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant4-benzyl-8-bromo-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-oneHCID 68578541—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyl-8-bromo-2,3,4,5-tetrahydrobenzo[f][1,4]oxazepineHCID 68578800100.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 4-benzyl-8-bromo-3,4-dihydro-1,4-benzoxazepine-5 (2H)-one (4.50 g, 13.5 mmol) in tetrahydrofuran (45 ml) was added 1M borane-tetrahydrofuran solution (54 ml, 54.0 mmol), and the mixture was stirred at 65° C. for 4 hr. Under ice-cooling, methanol (135 ml) and sodium hydroxide (11.7 g, 294 mmol) were added, and the mixture was stirred at room temperature for 1 hr. The solvent was evaporated under reduced pressure. The residue was poured into water and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the desired product (4.30 g, 100%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247403B2
Source datasetuspto-grants-2012_08
ORD IDord-aa36567726f14cf7980d6e00cbd6206e
Source noteuspto-grants-2012_08