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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168049Generated: October 28, 2026

Trityl chloride → (S)-4-benzyloxy-1-trityloxy-2-butanol

https://huagongshe.com/reaction/1168049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant(S)-4-Benzyloxy-1,2-butanediolHCID 9794180—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(S)-4-benzyloxy-1-trityloxy-2-butanolHCID 11015650100%

Reaction Steps

In toluene (100 ml) were dissolved (S)-4-benzyloxy-1,2-butanediol (25.8 g, 0.132 mol), triethylamine (20.2 ml, 0.145 mol) and 4-N,N-dimethylaminopyridine (DMAP) (0.80 g, 6.58 mmol). After cooling in ice bath, trityl chloride (36.69 g, 0.1316 mol) was added to the solution and the mixture was stirred at room temperature for 10 hours. The mixture was condensed in vacuo, diluted with ethyl acetate, washed with water and then saturated brine, dried on sodium sulfate, filtered and condensed in vacuo to give (S)-4-benzyloxy-1-trityloxy-2-butanol quantitatively (55.89, yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620977B1
Source datasetuspto-grants-2003_09
ORD IDord-f1587c997a9841998fb1cbfc8baf52ff
Source noteuspto-grants-2003_09