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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817628Generated: October 31, 2026

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

https://huagongshe.com/reaction/1817628

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 numberUS07598257B2
Source datasetuspto-grants-2009_10
ORD IDord-7b88ee6f6f50400f8e29cfc39c3d018c
Source noteuspto-grants-2009_10