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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229458Generated: October 26, 2026

N-t-butyl-3-benzoyloxy-1-pentanesulfonamide → HCID 18467564, compound

https://huagongshe.com/reaction/2229458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-t-butyl-3-benzoyloxy-1-pentanesulfonamideHCID 18467574—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 18467564HCID 1846756480.9%

Reaction Steps

A mixture of N-t-butyl-3-benzoyloxy-1-pentanesulfonamide (90.4 g) and trifluoroacetic acid (200 ml) was stirred overnight at room temperature. Trifluoroacetic acid was removed under reduced pressure and water and chloroform were added to the residue. A saturated aqueous solution of sodium hydrogencarbonate was added thereto with vigorously stirring until the aqueous layer became neutral. After extraction with chloroform, the organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate=2/1 to 1/1) to obtain 3-benzoyloxy-1-pentanesulfonamide (60.6 g) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420409B1
Source datasetuspto-grants-2002_07
ORD IDord-3249c274d15d48eaa429edd69d475f15
Source noteuspto-grants-2002_07