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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38681Generated: October 30, 2026

Ethyl 2-Cyano-2-methylpropionate → Ethyl 2-carbamothioyl-2,2-dimethylacetate

https://huagongshe.com/reaction/38681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-Cyano-2-methylpropionateHCID 344887—
ReactantDiphenyl-sulfanyl-sulfanylidene-$l^{5-phosphaneHCID 22486041—
SolventIsopropanolHCID 3776—
ProductEthyl 2-carbamothioyl-2,2-dimethylacetateHCID 1240983522.2%

Reaction Steps

A mixture of diphenyldithiophosphonic acid (ALFAAESAR, 1.42 g, 5.67 mmol) and 2-cyano-2-methylpropionic acid ethyl ester (ABCR, 0.412 mL, 2.83 mmol) in isopropanol (30 mL) was heated under reflux for 4 h. Reaction mixture was cooled to room temperature and a precipitate was formed. Reaction flask was placed in the freezer for 1 h. Reaction mixture was filtered and filtrate was concentrated. Residue was taken up in DCM (100 mL) and washed with water (20 mL), 1N NaOH (20 mL), saturated NaHCO3 (20 mL) and dried over sodium sulfate and concentrated. The resulting oil was loaded on a 25 g silica cartridge and eluted with linear gradient 0-50% hexane-ethyl acetate to yield the title compound (110 mg, 0.628 mmol, 22.2% yield). Another impure batch was loaded on a 10 g silica cartridge and eluted with linear gradient 0-50% hexane-ethyl acetate to recover the title compound (120 mg, 0.685 mmol, 24.17% yield). Total yield: (230 mg, 1.313 mmol, 46.32%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 9.70 (br s, 1H), 8.86 (br s, 1H), 4.05 (q, 2H), 1.39 (s, 6H), 1.15 (t, 3H). [ES+MS] m/z 176 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524750B2
Source datasetuspto-grants-2013_09
ORD IDord-0fa2f6cbb20a4225beef7778b22e2246
Source noteuspto-grants-2013_09