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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234213Generated: October 28, 2026

Trityl chloride → 4-trityloxybutan-1-ol

https://huagongshe.com/reaction/234213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
Reactant1,4-ButanediolHCID 8064—
SolventPyridineHCID 1049—
Product4-trityloxybutan-1-olHCID 37170241.6%

Reaction Steps

To a solution of 45 g of butane-1,4-diol in 0.25 of pyridine, cooled to 0° C., were added 139.4 g of triphenylchloromethane and the mixture was stirred at room temperature for 26 h. The precipitate formed was removed by filtration and the filtrate was evaporated in vacuo. The residue was taken up in 0.5 l of ethyl acetate and the solution was washed successively with 200 ml portions of water, 1N hydrochloric acid, water, 5% sodium bicarbonate solution and brine. The organic layer was dried over sodium sulfate and evaporated in vacuo. Crystallization of the residual material from ethyl acetate/hexane afforded 69.0 g of 4-trityloxy-1-butanol as white crystals of m.p. 73°-74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594135
Source datasetuspto-grants-1997_01
ORD IDord-e9af9902f91548aa823d4c01ddcf9eaa
Source noteuspto-grants-1997_01