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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351580Generated: October 30, 2026

Ethyl Acetate → 2,3-Dihydro-1,4-benzothiazine

https://huagongshe.com/reaction/351580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4H-1,4-Benzothiazin-3-oneHCID 21396—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2,3-Dihydro-1,4-benzothiazineHCID 15106496.5%

Reaction Steps

A solution of (2H)1,4-benzothiazin-3(4H)-one (20.0 g, 121.1 mmol) in anhydrous tetrahydrofuran (100 mL) was added to a stirred suspension of lithium aluminum hydride in anhydrous tetrahydrofuran (80 mL) under nitrogen at 0° C. The mixture was heated at reflux for 2 hrs and then poured into a mixture of ethyl acetate (300 mL) and ice (500 g). The organic layer was separated and the aqueous layer extracted with ethyl acetate. The combined organic layer was dried and concentrated under reduced pressure to provide 17.68 g (96.5%) of the desired compound which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743785B2
Source datasetuspto-grants-2004_06
ORD IDord-75c8e7adbdc94062972659bb58dc2fe8
Source noteuspto-grants-2004_06