Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377689Generated: October 31, 2026

Acetic Acid → 4H-1,4-Benzothiazin-3-one

https://huagongshe.com/reaction/1377689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantEthyl (2-aminophenyl)mercaptoacetateHCID 2736362—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,1-DichloroethaneHCID 6365—
Product4H-1,4-Benzothiazin-3-oneHCID 2139639.4%

Reaction Steps

Ethyl (2-aminophenyl)mercaptoacetate (322 mg, 1.52 mmole), N-tert-butyloxycarbonylpiperidin-4-one (456 mg, 2.29 mmole), acetic acid (478 ml, 8.36 mmole), and sodium triacetoxyborohydride (966 mg, 4.56 mmole) were combined in 10 ml of dichloroethane at room temperature, protected from moisture and stirred overnight. Saturated sodium bicarbonate solution was added and the reaction mixture was extracted with ethyl acetate. The combined extracts were washed with sodium bicarbonate solution and brine, then dried and concentrated. The crude product was chromatographed on silica gel (ethyl acetate-hexane elution, 1:3 v/v) to give 210 mg of the title compound along with 99 mg of 2H-1,4-benzothiazin-3(4H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665719
Source datasetuspto-grants-1997_09
ORD IDord-c07ec6b7ce2643b79ed519549334feea
Source noteuspto-grants-1997_09