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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723361Generated: October 31, 2026

Allyl bromide → HCID 21873363, compound

https://huagongshe.com/reaction/723361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium hydrideHCID 82127—
ReactantHCID 21873324HCID 21873324—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21873363HCID 21873363—

Reaction Steps

Potassium hydride (30% in oil, 40 mg) was added to a solution of 1-allyl-1-(4-benzyloxyphenyl)-3-(4-phenoxyphenyl)urea (133 mg) in THF (3 mL) at −78° C. After 30 minutes, allyl bromide (30 μL) was added. After 14 hours at room temperature, the solution was diluted with dichloromethane and washed with saturated sodium bicarbonate solution. The organic phase was dried and concentrated. The product with the molecular weight of 490.61 (C32H30N2O3); MS (ESI): 491 ([M+H]+), was obtained in this way.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141561B2
Source datasetuspto-grants-2006_11
ORD IDord-4aa67bc811bd45b88a69d51df4b33260
Source noteuspto-grants-2006_11