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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456365Generated: October 31, 2026

Trifluoromethanesulfonic anhydride → HCID 86753393, compound

https://huagongshe.com/reaction/1456365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 135977785HCID 135977785—
SolventPyridineHCID 1049—
ProductHCID 86753393HCID 8675339399.1%

Reaction Steps

8.4 ml (0.050 mol) of trifluoromethanesulphonic anhydride are added at 0° C. over 10 minutes to a solution of 11 g (0.042 mol) of (R)-5-(methoxymethyl)-3-(6-hydroxy-1,2-benzisoxazol-3-yl)oxazolidine-2-one in 110 ml of pyridine. The solution is stirred for 18 hours and then poured into ice-cold 2N aqueous hydrochloric acid solution. The product is extracted with ethyl acetate and then the organic phase is dried over sodium sulphate and concentrated under reduced pressure. 16.5 g of product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843975
Source datasetuspto-grants-1998_12
ORD IDord-ce9e47b6bef84735bd1f354e093fc833
Source noteuspto-grants-1998_12