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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352652Generated: November 1, 2026

Ethanol → HCID 56637441, compound

https://huagongshe.com/reaction/2352652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethyl iodideHCID 6328—
ReactantBenzenesulfonamideHCID 7370—
ReactantSodium HydroxideHCID 14798—
ReactantBenzonitrile, 4-isothiocyanato-HCID 17626—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 56637441HCID 5663744182.7%

Reaction Steps

A mixture of 5 g (0.031 mol) of 4-cyanophenyl isothiocyanate, of 6.3 g (0.04 mol) of benzenesulfonamide in 50 cm3 of acetone and of 1.6 g (0.04 mol) of sodium hydroxide in 3 cm3 of water is maintained for two hours at room temperature. The precipitate obtained is filtered, washed with acetone and ethyl ether (2×20 cm3). The final solid (9 g; yield 94%) is then placed in 50 cm3 of 95% ethanol containing 2.75 cm3 (0.044 mol) of methyl iodide. After 24 hours at room temperature the solution is concentrated to dryness and the residue is washed with ethyl ether (3×20 cm3) and dried in vacuo. 8.5 g (yield 80%) of N-(4-cyanophenyl)-N'-phenylsulfonyl-S-methylisothiourea (melting point 150° C.) is obtained: ##STR23##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877895
Source datasetuspto-grants-1989_10
ORD IDord-67ffcb328f6248c295c4867e760d20f4
Source noteuspto-grants-1989_10