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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596165Generated: October 29, 2026

Dichloromethane → HCID 21450746, compound

https://huagongshe.com/reaction/596165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAllyl bromideHCID 7841—
ReactantSodium BicarbonateHCID 516892—
Reactant7,7-Diphenyl-1,4-oxazepaneHCID 20326629—
ProductHCID 21450746HCID 21450746—

Reaction Steps

To the stirred solution of 5.06 g of 7,7-diphenyl-hexahydro-1,4-oxazepine in 50 ml of methylene chloride, 2.6 g of allyl bromide are added, followed by 40 ml of 10% aqueous sodium bicarbonate and the mixture is stirred for 24 hours at room temperature. The organic layer is separated, washed with water, dried, filtered and evaporated. The residue is taken up in acetone, the solution acidified with hydrogen chloride in acetone and diluted with diethyl ether, to yield the 4-allyl-7,7-diphenyl-hexahydro-1,4-oxazepine hydrochloride melting at 246° to 247°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04010166
Source datasetuspto-grants-1977_03
ORD IDord-66ea9860a23943669ddd612cac5b6dc2
Source noteuspto-grants-1977_03