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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501484Generated: November 1, 2026

Trityl chloride → 4-[2-(Trityloxy)ethyl]cyclohexanol

https://huagongshe.com/reaction/1501484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
Reactant4-(2-Hydroxyethyl)cyclohexan-1-olHCID 13751153—
SolventPyridineHCID 1049—
Product4-[2-(Trityloxy)ethyl]cyclohexanolHCID 57477970—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(2-Hydroxyethyl)cyclohexanol (crude from the previous reaction) (1.88 g, 0.0130 mol) was dissolved in pyridine (20.00 mL) and was cooled at 0° C. To the reaction was added triphenylmethyl chloride (4.0 g, 0.014 mol) and this mixture was stirred at 0° C. for 2 hours and at 25° C. for 16 hours. The reaction was concentrated using a rotary evaporator and the concentrate was extracted with ethyl acetate. The organic extracts were washed with water, and saturated NaCl, then dried (MgSO4) and concentrated in vacuo. The concentrate was chromatographed on silica gel (30% EtOAc/hexanes) to give the trans isomer (1.98 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206187B2
Source datasetuspto-grants-2015_12
ORD IDord-a0858ffcf2404de0b210acbc55b219cc
Source noteuspto-grants-2015_12