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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857704Generated: November 1, 2026

Boron Trichloride → HCID 22130250, compound

https://huagongshe.com/reaction/1857704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22130396HCID 22130396—
SolventDichloromethaneHCID 6344—
ProductHCID 22130250HCID 2213025013%

Reaction Conditions

Temperature-40 °C

Reaction Steps

In 5 ml of methylene chloride was dissolved 470 mg (1.13 mmol) of 1-allyl-2-benzyloxymethyl-5-(3-chlorophenylthio)-4-isopropyl-1H-imidazole (17g), with cooling to -40° C., 0.7 ml (1.36 mmol) of methylene chloride solution of boron trichloride (1.94 molar) was added with stirring, and the mixture was stirred for 30 minutes. To this reaction mixture, a saturated aqueous solution of sodium bicarbonate was added for neutralization, methylene chloride layer was washed with water arid dried over sodium sulfate. The solvent was concentrated under reduced pressure and the residue was fractionated by silica gel chromatography (ethyl acetate: methylene chloride=1:4). From the first fraction, 50 mg (yield 13%) of 1-allyl-2-chloromethyl-5-(3-chlorophenylthio)-4-isopropylimidazole (28a) was obtained as oil, and then, 155 mg (yield 43%) of Compound I-17 was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147097
Source datasetuspto-grants-2000_11
ORD IDord-97bf25d32eec408b8294bdd860b1c83d
Source noteuspto-grants-2000_11