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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326333Generated: October 30, 2026

Triethylamine → Ethyl 2-chloro-5-[(6-ethyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoate

https://huagongshe.com/reaction/326333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 5-amino-2-chlorobenzoateHCID 13226857—
Reactant2-Ethyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acidHCID 21470250—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-chloro-5-[(6-ethyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoateHCID 46581058%

Reaction Conditions

Temperature35 °C

Reaction Steps

Thionyl chloride (4.0 g, 0.034 mole) was added to a stirred mixture of 2-ethyl-5,6-dihydro-1,4-oxathiin-3-carboxylic acid (5.9 g, 0.034 mole) and methylene chloride (100 ml). The mixture was warmed to about 35° C. for 3 hours, then evaporated under reduced pressure. The residue, crude 2-ethyl-5,6-dihydro-1,4-oxathiin-3-carbonyl chloride, was dissolved in methylene chloride (100 ml), and the ice-chilled solution treated dropwise with a solution of ethyl 5-amino-2-chlorobenzoate (6.8 g, 0.034 mole) and triethylamine (3.7 g, 0.037 mole) in methylene chloride (100 ml). The reaction mixture was stirred overnight at room temperature and then worked up by washing in sequence with water, dilute hydrochloric acid, water, 2% sodium hydroxide and water. Evaporation of the solvent left an oil, which solidified. After recrystallization from ethanol (30 ml) the product (7.0 g, 58% yield) melted at 86°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05268389
Source datasetuspto-grants-1993_12
ORD IDord-49e93c7e7f824611b36fe9524466451f
Source noteuspto-grants-1993_12