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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841754Generated: November 2, 2026

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

https://huagongshe.com/reaction/841754

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-hydroxyrnethyl-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 numberUS06369261B1
Source datasetuspto-grants-2002_04
ORD IDord-b3f63b1971a6481a921d7a8ec3bce50e
Source noteuspto-grants-2002_04