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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195788Generated: November 5, 2026

Benzyl Bromide → HCID 53995652, compound

https://huagongshe.com/reaction/1195788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 54017563HCID 54017563—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53995652HCID 5399565271%

Reaction Steps

To a solution of 3-ethyl-2,3,9,10,11,12-hexahydro-1H-quino[4,3,2-ef][1,4]benzoxazepine (5.0 g) in dry tetrahydrofuran (150 ml) was added potassium t-butoxide (3.0 g). The mixture was stirred for 15 mins, benzyl bromide (3.16 ml) was added, and the reaction mixture was stirred at room temperature overnight. The reaction mixture was heated at reflux for 1.5 hrs, allowed to cool, concentrated and diluted with saturated sodium bicarbonate solution (250 ml). The mixture was extracted twice with ethyl acetate (250 ml), and the organic extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated. Trituration of the residue first with pentane and then diethyl ether, gave 4.65 g (71%) of 1-benzyl-3-ethyl-1,3,9,10,11,12-hexahydro-2H-quino[4,3,2-ef][1,4]benzoxazepin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112829
Source datasetuspto-grants-1992_05
ORD IDord-7a75203a8ead45e4ac7499dafcaac4d4
Source noteuspto-grants-1992_05