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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987821Generated: October 27, 2026

Trifluoromethanesulfonic anhydride → 3-(2-Oxotetrahydrofuran-3-ylthio)propyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1987821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant2,6-Di-tert-butylpyridineHCID 68510—
Reactant3-(3-Hydroxypropylsulfanyl)-dihydrofuran-2-oneHCID 66115662—
SolventDichloromethaneHCID 6344—
Product3-(2-Oxotetrahydrofuran-3-ylthio)propyl trifluoromethanesulfonateHCID 86606510—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triflic anhydride (0.544 ml, 3.23 mmol) was added to a pre-cooled (0° C.) solution of 2,6-di-tert-butylpyridine (1.61 ml, 7.15 mmol) in methylene chloride (16 mL). A solution of 3-(3-hydroxypropylthio)-dihydrofuran-2(3H)-one (0.600 g, 3.41 mmol) dissolved in methylene chloride (2.5 mL) was added dropwise. The reaction was stirred at 0° C. for 15 minutes. The product was utilized in the subsequent step without isolation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553842B2
Source datasetuspto-grants-2009_06
ORD IDord-cf9bb120347942699a197011e4357ec8
Source noteuspto-grants-2009_06