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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938849Generated: October 30, 2026

Thionyl Chloride → HCID 507310, compound

https://huagongshe.com/reaction/1938849

Reaction equation

Participants

RoleNameHCIDCharge
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%

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 tziethylamine (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 numberUS05693827
Source datasetuspto-grants-1997_12
ORD IDord-175bbec288ce4b0ca20a1582a8ae151c
Source noteuspto-grants-1997_12