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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105536Generated: October 31, 2026

Acetic Anhydride → HCID 86600475, compound

https://huagongshe.com/reaction/2105536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 86600474HCID 86600474—
SolventFormic AcidHCID 284—
SolventEthyl AcetateHCID 8857—
ProductHCID 86600475HCID 8660047581%

Reaction Steps

To a solution of 2-(benzyloxyamino-methyl)-4H-benzo[1,4]thiazin-3-one (2.96 mmol) in 15 mL of formic acid at 0° C., acetic anhydride is added (15.1 mmol) and the reaction is stirred at room temperature overnight. The mixture is diluted with EtOAc and washed with water followed by brine and NaHCO3. Purification by column chromatography (hexane/EtOAc) gives N-benzyloxy-N-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-ylmethyl)-formamide. Yield: 81%. MS: (ES+): 329.2 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579363B2
Source datasetuspto-grants-2009_08
ORD IDord-c2e52dc313b94540aefe178984c11cb9
Source noteuspto-grants-2009_08