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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181012Generated: October 29, 2026

Acetic Anhydride → HCID 22484967, compound

https://huagongshe.com/reaction/2181012

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-hydroxybutane-sulfonamide 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 numberUS06890934B2
Source datasetuspto-grants-2005_05
ORD IDord-36512cf2f46d426e8d26832aeb5028d7
Source noteuspto-grants-2005_05