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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851921Generated: October 28, 2026

Acetic Anhydride → HCID 86600475, compound

https://huagongshe.com/reaction/851921

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 numberUS07253164B2
Source datasetuspto-grants-2007_08
ORD IDord-cbc9fd7bcfaa42338f4c62ef0b18bb14
Source noteuspto-grants-2007_08