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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326335Generated: October 30, 2026

Triethylamine → HCID 507310, compound

https://huagongshe.com/reaction/326335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acidHCID 539946—
ReactantEthyl 3-amino-4-methylbenzoateHCID 12607966—
SolventDichloromethaneHCID 6344—
ProductHCID 507310HCID 50731059.7%

Reaction Steps

Thionyl chloride (4.5 g, 0.038 mole) was added to a stirred mixture of 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxylic acid (6.0 g, 0.037 mole) and methylene chloride (100 ml . The mixture was warmed to 30°-35° C. for 3 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 ethyl 3-amino-4-methylbenzoate (6.7 g, 0.037 mole) and triethylamine (4.0 g, 0.040 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 gave an oil, which solidified. After recrystallization from ethanol (30 ml), the product (7.1 g, 59% yield) melted at 105°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05268389
Source datasetuspto-grants-1993_12
ORD IDord-6827f29854b643339c800e99256b71a5
Source noteuspto-grants-1993_12