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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030242Generated: November 4, 2026

Ethyl Acetate → HCID 54056685, compound

https://huagongshe.com/reaction/1030242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
ReactantHCID 10922900HCID 10922900—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54056685HCID 5405668571%

Reaction Steps

A solution of diethyl cyanomethylphosphonate (215 mg, 1.2 mmol) at room temperature in dry tetrahydrofuran (20 ml) was treated with a 60% oil dispersion of sodium hydride (40 mg, lmmol). After 15 mins at room temperature (±)-N-methyl-2 -oxo-1-(pyrid-3 -yl)cyclohexane carbothioamide (245 mg, lmmol) was added and the resulting solution stirred for 3 hours at room temperature. Ethyl acetate (50 ml) and then water (50 ml) were added to the reaction mixture. The layers were separated and the organics washed with water (50 ml). The organic extract was dried over magnesium sulphate and concentrated in vacuo to give a crude gum. Purification by flash chromatography, eluting with a 1:1 (v/v) mixture of ethyl acetate/hexane gave (±)-2 -cyanomethylene-N-methyl-1-(pyrid-3 -yl)cyclohexane carbothioamide as a colourless gum (190 mg, 0.7 mmol). Trituration with ether yielded a white solid (190 mg, 0.7 mmol), m.p. 182°-183° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104883
Source datasetuspto-grants-1992_04
ORD IDord-bdd806e8b41d456ba5e81d5d27113b23
Source noteuspto-grants-1992_04