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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938845Generated: October 31, 2026

Triethylamine → HCID 465809, compound

https://huagongshe.com/reaction/1938845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactantisopropyl 3-aminobenzoateHCID 236743—
Reactant2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acidHCID 539946—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 465809HCID 46580942.9%

Reaction Steps

Thionyl chloride (3.5 g, 0.029 mole) was added to a stirred mixture of 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxylic acid (4.7 g, 0.029 mole) and methylene chloride (100 ml). The mixture was warmed to 30°-35° C. for 4 hours, then evaporated under reduced pressure. The residue, crude 5,6-dihydro-2-methyl-1,4-oxathiin-3-carbonyl chloride, was dissolved in methylene chloride (100 ml), and the ice-chilled solution treated dropwise with a solution of 1-methylethyl 3-aminobenzoate (5,.2 g, 0.029 mole) and triethylamine (2.9 g, 0.029 mole) in methylene chloride (50 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 (4.0 g, 42% yield) melted at 92°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693827
Source datasetuspto-grants-1997_12
ORD IDord-90e45774744b44b68e872e5d0e88e619
Source noteuspto-grants-1997_12