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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374369Generated: November 2, 2026

Trityl chloride → HCID 86596908, compound

https://huagongshe.com/reaction/1374369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantHCID 86596907HCID 86596907—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86596908HCID 86596908—

Reaction Steps

A sample of benzyl (1S,2R,4R)-4hydroxy-2-(hydroxymethyl)cyclohexylcarbamate (8.78 g, 31.42 mMol) was dissolved in anhydrous CH2Cl2 prior to the addition of triethylamine (11 mL, 78.55 mMol) followed by DMAP (0.05 g) and then trityl chloride (10.52 g, 37.7 mMol) in one portion. The reaction mixture was stirred at rt overnight. The reaction was partitioned between CH2Cl2 and water. The organic layer was washed with brine and dried (MgSO4), filtered, concentrated and chromatographed. Benzyl (1S,2R,4R)-4-hydroxy-2-(trityloxymethyl)cyclohexylcarbamate was obtained as a white foamy solid (9.85 g, yield=60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163937B2
Source datasetuspto-grants-2007_01
ORD IDord-0655bb0532ca4f41b85f3aaf69baab81
Source noteuspto-grants-2007_01