Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750560Generated: October 31, 2026

Malononitrile → 2-Cyano-thioacetimidic acid 4-methoxy-benzyl ester

https://huagongshe.com/reaction/750560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalononitrileHCID 8010—
ReactantSodium HydroxideHCID 14798—
Reactant4-Methoxy-alpha-toluenethiolHCID 80407—
SolventWaterHCID 962—
SolventAmmonium ChlorideHCID 25517—
SolventWater ethanolHCID 19096565—
Product2-Cyano-thioacetimidic acid 4-methoxy-benzyl esterHCID 2057719360.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of sodium hydroxide (13 g, 0.32 mol) in 750 mL of 1:1 ethanol-water at 0° C. was added 4-methoxybenzylmercaptan (50 g, 0.324 mol) and malononitrile (21 g, 0.324 mol). After stirring for 3 hours at 0° C., the mixture was diluted with 500 mL of saturated aqueous NH4Cl, diluted with 4 l of water and filtered. The solids were washed with ether, and the filtrated was diluted with an equal volume of hexane and filtered. The combined solids were dried in vacuo, affording 43 g (60%) of 2-cyano-thioacetimidic acid 4-methoxy-benzyl ester as a colorless solid. 1H NMR (400 MHz, CDCl3) δ 7.22 (d, 2H, J=7.6 Hz), 6.84 (d, 2H, J=8.8 Hz), 4.74 (bs, 1H), 3.98 (s, 2H), 3.78 (s, 3H) ppm; MS (APCl, m/z): 221 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405218B2
Source datasetuspto-grants-2008_07
ORD IDord-ee2ad3d4432843aaad94a8a008a8face
Source noteuspto-grants-2008_07