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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236045Generated: October 29, 2026

Water → Acetic acid, [(1-thioxoethyl)thio]-, ethyl ester

https://huagongshe.com/reaction/2236045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbon DisulfideHCID 6348—
ReactantEthyl bromoacetateHCID 7748—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
ProductAcetic acid, [(1-thioxoethyl)thio]-, ethyl esterHCID 9898991—

Reaction Conditions

Temperature40 °C

Reaction Steps

Methyl magnesium chloride (10 mL, 3M solution in THF) was diluted with THF (10 mL) and the resulting solution warmed to 40° C. Carbon disulfide (2.28 g, 0.03 mol) was added over 10 minutes while maintaining the reaction temperature at 40° C. The reaction was cooled to room temperature before adding ethyl bromoacetate (5.01 g, 0.03 mol) over 15 minutes. The reaction temperature was increased to 50° C. and maintained for a further 4 hours. Water (100 mL) was added and the organic products were extracted with ethyl acetate (3×60 mL) The combined organic extracts were washed with water, brine and dried over anhydrous magnesium sulfate. After removal of solvent and column chromatography (Kieselgel-60, 70-230 mesh, 10% diethyl ether in n-hexane eluent), pure ethoxycarbonylmethyl dithioacetate was obtained as a golden oil (1.3 g, 24.3% yield). 1H-nmr (CDCl3) d (ppm): 1.25 (t, 3H); 2.90 (s, 3H); 4.07 (s, 2H) and 4.20 (q, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714075B1
Source datasetuspto-grants-2010_05
ORD IDord-0ef665568d404097a1193d5b9f4f7528
Source noteuspto-grants-2010_05