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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655081Generated: November 2, 2026

Methyl thiocyanate → HCID 20077557, compound

https://huagongshe.com/reaction/1655081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl thiocyanateHCID 11168—
ReactantSodium HydroxideHCID 14798—
ReactantBoron TrichlorideHCID 25135—
Reactant4-EthylphenolHCID 31242—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 20077557HCID 20077557—

Reaction Conditions

Temperature4 °C

Reaction Steps

A solution of 4-ethylphenol (2.44 g) in dichloromethane (10 ml), was added to a stirred, ice-cooled, solution of 1M boron trichloride in dichloromethane (24 ml) under argon, followed by methylthiocyanate (1.64 ml), and then anhydrous aluminium chloride (2.66 g). The mixture was stirred for 1 hour at 4° C., then heated at reflux (bath temperature 60° C.) for 4 hours and finally stirred for 16 hours at ambient temperature. The mixture was added cautiously to a stirred, ice-cooled, 4M sodium hydroxide solution and the resultant mixture heated at 70° C. for 30 minutes then cooled. The aqueous phase was separated, washed with dichloromethane (2×25 ml), then acidified to pH2 with 6M hydrochloric acid and extracted with ethyl acetate (3×75 ml). The combined organic extracts were washed with saturated brine (3×50 ml), dried (MgSO4) and the solvent removed in vacuo to give a brown solid. Purification by flash chromatography, eluting with 20% v/v ethyl acetate in hexane, followed by recrystallisation from hexane gave 2-cyano-4-ethylphenol (A) (2.56 g), m.p. 95°-98° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05410064
Source datasetuspto-grants-1995_04
ORD IDord-bf3e41565fe74c51a768f95a184fa89e
Source noteuspto-grants-1995_04