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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600933Generated: October 30, 2026

HCID 57437675, compound → HCID 57437676, compound

https://huagongshe.com/reaction/600933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57437675HCID 57437675—
ReactantHCID 178419663HCID 178419663—
SolventDichloromethaneHCID 6344—
ProductHCID 57437676HCID 57437676—

Reaction Steps

A solution of pyridin-4-yl(1-trityl-1H-imidazol-5-yl)methanone (500 mg, 1.19 mmol) in dichloromethane (25 mL) at room temperature was treated with benzyl magnesium bromide (0.595 mL, 1.78 mmol, 3M in ether) and allowed to react at room temperature and the reaction mixture was then stirred at room temperature for 16 hours. The mixture was quenched with water (20 mL) and a saturated solution of ammonium chloride (20 mL). The residue was isolated in a typical aqueous to give pyridin-4-yl(1-trityl-1H-imidazol-5-yl)methanol, (Intermediate 4) (526 mg, crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902247B2
Source datasetuspto-grants-2011_03
ORD IDord-f1226b495f6e4306bdea9efb4808b4f0
Source noteuspto-grants-2011_03