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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407871Generated: October 26, 2026

Acetic Acid → HCID 53627664, compound

https://huagongshe.com/reaction/407871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanethiolHCID 6343—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-((4R)-2,2-dimethyl-5-oxo-1,3-dioxolan-4-yl)acetic acidHCID 10844960—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 53627664HCID 5362766471.8%

Reaction Steps

(R)-2-(2,2-Dimethyl-5-oxo-1,3-dioxolan-4-yl)acetic acid (25 g, 144 mmol) was dissolved in CH2Cl2 (500 mL) and cooled in an ice bath. Ethanethiol (21.2 mL, 287 mmol) and N,N-dimethylpyridin-4-amine (0.351 g, 2.87 mmol) were added followed by DCC (35.5 g, 172 mmol). This mixture was stirred in ice bath for 1 hour, and then 2 hours at ambient temperature. Acetic acid (45 mL) was added and then stirred the mixture for 10 minutes. The reaction mixture was then poured into vigorously stirred ether (400 mL) and filtered. The filtrate was washed with 10% sodium carbonate, water, 0.5 N HCl, water and brine. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified over silica gel (1-5-10% EtOAc in hexanes) to afford (R)—S-ethyl 2-(2,2-dimethyl-5-oxo-1,3-dioxolan-4-yl)ethanethioate (22.5 g, 103 mmol, 71.8% yield) as a clear colorless oil that solidified to a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-f2be078a86ea4a7aaf772ca9c1280ad2
Source noteuspto-grants-2014_06