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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326332Generated: October 28, 2026

Triethylamine → HCID 465809, compound

https://huagongshe.com/reaction/326332

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. Analysis: Calc.: C 59.79, H 5.96, N 4.36, Found: C 59.46, H 6.21, N 4.51

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05268389
Source datasetuspto-grants-1993_12
ORD IDord-5ea1d1f5095d41dea5f98b013b7502e1
Source noteuspto-grants-1993_12