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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255834Generated: October 31, 2026

Trifluoroacetic acid → HCID 13923713, compound

https://huagongshe.com/reaction/255834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 15616509HCID 15616509—
ProductHCID 13923713HCID 1392371381.9%

Reaction Steps

The product from Example 5 (13.8 g) was added in portions to 75 ml of trifluoroacetic acid at room temperature and the resulting solution was stirred for 21 hours. Removal of the trifluoroacetic acid in vacuo gave a light orange oil which crystallized upon addition of diethyl ether. Filtration and air drying yielded 9.18 g of pure 2-[2-(acetyloxy)ethyl]benzenesulfonamide as a white powder, m.p. 116°-117.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699650
Source datasetuspto-grants-1987_10
ORD IDord-c9ba7d3c50f14375a8abcb9e0e0cec5e
Source noteuspto-grants-1987_10