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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422379Generated: November 2, 2026

Thionyl Chloride → 4-(Chloromethyl)-1-trityl-1H-imidazole

https://huagongshe.com/reaction/2422379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant[1-(triphenylmethyl)-1H-imidazol-4-yl]methanolHCID 382182—
SolventDichloromethaneHCID 6344—
Product4-(Chloromethyl)-1-trityl-1H-imidazoleHCID 2763176114.1%

Reaction Steps

To a suspension of 4-hydroxymethyl-1-tritylimidazole (6.13 g, 18 mmol) in dichloromethane (75 mL), cooled using an ice/water, was added dropwise thionyl chloride (5.0 g, 42 mmol) over 6 min. The ice/water bath was removed and the reaction was stirred for an additional 30 min. The DCM and SOCl2 were removed under reduced pressure. The resulting solid was triturated with diisopropyl ether (200 mL), collected by filtration and dried in vacuo to give 7.37 g (>100%) of 83% pure 4-(chloromethyl)-1-trityl-1H-imidazole; retention time, 7.33 min.; column: YMC ODS-A (3 μm, 50×4.6 mm); gradient: 10% to 100% B in A over 10 min. at 1.25 mL/min. Solvent A: 0.1% TFA in water, Solvent B: 0.1% TFA in AcCN. LC/MS: ESI (M+H)+=359.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960349B2
Source datasetuspto-grants-2011_06
ORD IDord-42e2e2ef73c44a9b87b6ae75bac288e9
Source noteuspto-grants-2011_06