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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754978Generated: October 28, 2026

Boron Trichloride → HCID 66816495, compound

https://huagongshe.com/reaction/1754978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66816899HCID 66816899—
SolventDichloromethaneHCID 6344—
ProductHCID 66816495HCID 6681649584%

Reaction Steps

Boron trichloride (0.93 ml, 0.93 mmol, 1.0 M solution in dichloromethane) was added to a solution of 1-(2-(benzyloxy)ethyl)-1-(4-bromo-3,5-dimethylphenyl)-3-(2-hydroxyethyl)urea (98 mg, 0.23 mmol) in anhydrous dichloromethane (4.6 ml) at −78° C., and the mixture was stirred at the same temperature for two hours. A saturated aqueous sodium bicarbonate solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic phase was sequentially washed with water and saturated brine and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (dichloromethane-methanol) to give 1-(4-bromo-3,5-dimethylphenyl)-1,3-bis(2-hydroxyethyl)urea (64 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-21837ce94fa04eb9a1b39264d71737b2
Source noteuspto-grants-2015_10