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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650599Generated: October 29, 2026

Ethyl Acetate → HCID 21712759, compound

https://huagongshe.com/reaction/650599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantButyl iodideHCID 10962—
ReactantHCID 21712662HCID 21712662—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 21712759HCID 21712759—

Reaction Steps

To a solution of 6-cyano-2,3-dihydro-2-oxo-1H-thieno[2,3-b][1,4]thiazine (13.6 g) in N,N-dimethylformamide (270 ml) was added potassium tert-butoxide (9.3 g) under ice cooling. After stirring for 10 minutes under ice cooling, to the reaction mixture was added 1-iodobutane (9.5 ml). After stirring for 8 hours at room temperature, the reaction mixture was poured into a mixture of ethyl acetate and water. The organic layer was successively washed with water and brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was purified by column chromatography on silica gel eluting with chloroform. The fractions containing the object compounds were collected and evaporated in vacuo to give 1-n-butyl-6-cyano-2,3-dihydro-2-oxo-1H-thieno[2,3-b][1,4]thiazine (13.78 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274619B1
Source datasetuspto-grants-2001_08
ORD IDord-b20ec7b3ef3740ac84705cf6ed09e340
Source noteuspto-grants-2001_08