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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326330Generated: October 30, 2026

Triethylamine → HCID 507307, compound

https://huagongshe.com/reaction/326330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 3-aminobenzoateHCID 11400—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acidHCID 539946—
SolventDichloromethaneHCID 6344—
ProductHCID 507307HCID 50730773%

Reaction Steps

Thionyl chloride (6.5 g, 0.055 mole) was added to a stirred mixture of 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxylic acid (8.0 g, 0.050 mole) and methylene chloride (50 ml). The mixture was warmed to 35°-40° C. for hours and the resulting dark solution evaporated under reduced pressure. The solid residue, crude 5,6-dihydro-2-methyl-1,4-oxathiin-3-carbonyl chloride, was dissolved in methylene chloride (50 ml). On the following day, the solution was treated dropwise at 5°-20° C. over 2 hours with a solution of ethyl 3-aminobenzoate (8.2 g, 0.050 mole) and triethylamine (5.5 g, 0.054 mole) in methylene chloride (50 ml). The reaction mixture was stirred at room temperature for a further 5 hours and worked up by washing in sequence with water (50 ml), dilute hydrochloric acid (3.5%, 50 ml), water (50 ml), dilute sodium hydroxide (2%, 25 ml) and water (50 ml). Evaporation of the solvent left an oil, which slowly solidified. Recrystallization from ethanol 75 ml gave yellow-tan crystals, m.p. 100° -102° C. (11.2 g, 73% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05268389
Source datasetuspto-grants-1993_12
ORD IDord-7f7d693bea1e4d1d8a24409909fbe53a
Source noteuspto-grants-1993_12