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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368220Generated: November 2, 2026

Acetic Anhydride → HCID 22484967, compound

https://huagongshe.com/reaction/1368220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 22484955HCID 22484955—
SolventPyridineHCID 1049—
ProductHCID 22484967HCID 22484967—

Reaction Steps

A crude product (1.17 g) of N-tert-butyl-4-hydroxybutanesulfonamide was dissolved in pyridine (3.0 ml) and acetic anhydride (1.5 ml) was added, and the mixture was left standing at room temperature for 1 hr. The reaction mixture was concentrated to dryness under reduced pressure and the residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed once with water and once with saturated brine, dried over magnesium sulfate and concentrated to dryness under reduced pressure to give N-tert-butyl-4-acetoxybutanesulfonamide (425 mg) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573274B1
Source datasetuspto-grants-2003_06
ORD IDord-ac3321f02a7545e0a38ecc1ae20b35ea
Source noteuspto-grants-2003_06