Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24263Generated: October 29, 2026

Pyridine → 2-Isopropyl-4-trifluoromethylsulfonyloxy-benzyl acetate

https://huagongshe.com/reaction/24263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
Reactant4-Hydroxymethyl-3-isopropyl-phenyl 1,1,1-trifluoro-methanesulfonateHCID 22568893—
SolventDichloromethaneHCID 6344—
Product2-Isopropyl-4-trifluoromethylsulfonyloxy-benzyl acetateHCID 18740708—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-hydroxymethyl-3-isopropylphenyl 1,1,1-trifluoromethanesulfonate (Intermediate 149, 190.0 mg, 0.64 mmol) in 5 mL CH2Cl2 was added acetyl chloride (75.0 mg, 0.96 mmol) and pyridine(101.0 mg, 1.38 mmols). After stirring for 3 hours at 25° C. the reaction was quenched by the addition of H2O and the resulting mixture extracted with EtOAc. The combined organic layers were washed with H2O and saturated aqueous NaCl, dried (MgSO4) and concentrated under reduced pressure. The title compound, 182 mg (84%), was isolated from the residual oil by column chromatography (5-10% EtOAc—hexanes) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855512B2
Source datasetuspto-grants-2005_02
ORD IDord-7b5f23c000fd44a5962e150845024967
Source noteuspto-grants-2005_02