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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194993Generated: October 30, 2026

Hydrochloric Acid → HCID 58988191, compound

https://huagongshe.com/reaction/2194993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl formateHCID 8025—
ReactantN-(7-Oxo-4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)acetamideHCID 597793—
ReactantSodium MethoxideHCID 10942334—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
ProductHCID 58988191HCID 58988191—

Reaction Conditions

Temperature0 °C

Reaction Steps

20 g (0.37 mol) sodium methoxide are suspended in 50 mL dimethylformamide, a suspension of 21 g (0.1 mol) N-(7-oxo-4,5,6,7-tetrahydro-benzothiazol-2-yl)-acetamide in 100 mL dimethylformamide is added dropwise. The mixture is stirred for 15 minutes, then cooled to 0° C. A mixture of 29.9 mL (0.37 mol) ethyl formate and 60 mL benzene is added dropwise and the reaction mixture is diluted with another 100 mL benzene. A precipitate gradually settles out and stirring is continued at 0° C. for 3.5 hours. The suspension is hydrolysed with 370 mL 1 molar hydrochloric acid, the solid precipitated is suction filtered. The two phases of the mother liquor are separated, the aqueous phase is extracted with dichloromethane. The resulting organic phase is dried and evaporated to dryness. The solid and the residue from the extraction are recrystallised from acetonitrile. Yield: 20 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334378B2
Source datasetuspto-grants-2012_12
ORD IDord-9928775d2d9347ebb951bec6a8803dfc
Source noteuspto-grants-2012_12