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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416000Generated: November 4, 2026

Boron Trichloride → HCID 22130250, compound

https://huagongshe.com/reaction/1416000

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

(2)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 addled 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 and 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. mp 84-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910506
Source datasetuspto-grants-1999_06
ORD IDord-f30a24d544d943a4837291976e8460e0
Source noteuspto-grants-1999_06