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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702872Generated: October 27, 2026

Triethylamine → 5-[(Carbethoxymethyl)carbamoyloxy]-1,3-benzoxathiol-2-one

https://huagongshe.com/reaction/1702872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl isocyanatoacetateHCID 76283—
Reactant1,3-Benzoxathiol-2-one, 5-hydroxy-HCID 139067—
SolventMethyl Ethyl KetoneHCID 6569—
Product5-[(Carbethoxymethyl)carbamoyloxy]-1,3-benzoxathiol-2-oneHCID 13053836—

Reaction Steps

5-hydroxy-1,3-benzoxathiol-2-one (14.0 grams), was mixed with ethyl isocyanatoacetate (11.9 grams) and 0.84 gram of triethylamine in 165 milliliters of methyl ethyl ketone. The resulting mixture was then heated at reflux temperature for one hour and ten minutes and was allowed to cool and stand at ambient temperature for 15 hours. The solvent was then removed by evaporation in vacuo. The white, solid residue was recrystallized from a solution of 2% ethyl acetate in carbon tetrachloride. The resulting white crystalline solid had a melting point of 94.5°-96.5° C. This product was then recrystallized from a mixture of ethyl acetate and methylcyclohexane to give the desired purified product, 5-[(carbethoxymethyl)-carbamoyloxy]-1,3-benzoxathiol-2-one as colorless crystals having a melting point of 97.5°-98.5° C. Elemental analysis calculated for C12H11NO6S (percent): carbon--48.48; hydrogen--3.73; nitrogen--4.71. Found: carbon--48.6; hydrogen--3.84; nitrogen--4.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04349685
Source datasetuspto-grants-1982_09
ORD IDord-fbad1ff8df7c43829839f603b1d9d8c1
Source noteuspto-grants-1982_09