Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439867Generated: October 26, 2026

Thiophene → 3-oxo-2-(2-thienyl)-3,4-dihydro-2H-1,4-benzothiazine

https://huagongshe.com/reaction/1439867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
Reactant2H-1,4-Benzothiazin-3(4H)-one, 2-chloro-HCID 12218599—
SolventDichloromethaneHCID 6344—
Product3-oxo-2-(2-thienyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 1898440670.3%

Reaction Steps

To a solution of 2-chloro-3-oxo-3,4-dihydro-2H-1,4-benzothiazine (9.38 g) and thiophene (7.91 g) in methylene chloride (250 ml) is added in portions stannic chloride (12.2 g) at 0° to 5° C. After stirring at the same temperature for 45 minutes, the mixture is poured into ice water, and the organic layer is separated. The aqueous layer is extracted with ethyl acetate, and the ethyl acetate layer is combined with the above organic layer and distilled to remove the solvent. The resulting solid material is recrystallized from ethanol to give 3-oxo-2-(2-thienyl)-3,4-dihydro-2H-1,4-benzothiazine (8.17 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05496815
Source datasetuspto-grants-1996_03
ORD IDord-447649090ebb4efdb257883de18da4a2
Source noteuspto-grants-1996_03