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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890665Generated: October 30, 2026

Hydrochloric Acid → HCID 21866758, compound

https://huagongshe.com/reaction/890665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantHCID 23706078HCID 23706078—
SolventAcetic AnhydrideHCID 7918—
Solvent3-MethylpyridineHCID 7970—
ProductHCID 21866758HCID 21866758—

Reaction Steps

To 44.0 ml of a suspension of 16.70 g of sodium 2-(2-thenoylamino)acetate in β-picoline, 42.7 ml of acetic anhydride was added, and stirred for 3 hours at room temperature. After ice-cooling, 26.3 ml of ethanol, 129.7 ml of water and 45.2 ml of conc. hydrochloric acid were slowly added dropwise in sequence, and the mixture was stirred for 15 minutes as it is. After removal of ice-bath, the mixture was stirred for another 15 minutes at room temperature. Water (250 ml) was added and the precipitated crystals were collected, and washed with water. To the crystals was added 37.0 ml of water, and the mixture was heated to reflux for 1 hour. After 14.0 g of sodium chloride was added, the mixture was heated to reflux for another 1 hour. The reaction solution was extracted with ethyl acetate, and dried over anhydrous magnesium sulfate. After addition of activated carbon (Kyoryoku-sirasagi® MOIWY433), the mixture was stirred for 30 minutes at room temperature. The solvent was distilled off under reduced pressure. The residue was crystallized by addition of t-butyl methyl ether to provide 7.15 g of the objective compound as pale brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06998412B2
Source datasetuspto-grants-2006_02
ORD IDord-dea9f7f8378645a59ffb47fb3eb7ed00
Source noteuspto-grants-2006_02