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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365781Generated: October 26, 2026

Pyridine → (+/-)-2-Acetoxy-5-(p-Toluenesulfonyloxymethyl)-Tetrahydrofuran

https://huagongshe.com/reaction/365781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant(+/-)2-Hydroxy-5-(p-Toluenesulfonyloxymethyl)-TetrahydrofuranHCID 21255848—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(+/-)-2-Acetoxy-5-(p-Toluenesulfonyloxymethyl)-TetrahydrofuranHCID 21255879—

Reaction Steps

To a stirring solution of (±)2-hydroxy-5-(p-toluenesulfonyloxymethyl)-tetrahydrofuran (example 58) (4.20 g, 15.44 mmol), pyridine (2.75 mL, 33.97 mmol) and DMAP (catalytic) in methylene chloride (100 mL) at rt was added acetic anhydride (2.91 mL, 30.88 mmol). After stirring the solution for 1 h, it was washed with water (50 mL), 1 N HCl (50 mL), saturated NaHCO3 (50 mL), dried (MgSO4) and concentrated to give the title compound as a 1:1 mixture of cis and trans isomers (4.85 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127540
Source datasetuspto-grants-2000_10
ORD IDord-ffd578d93a914608bcaf19943f5c2df3
Source noteuspto-grants-2000_10