Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492351Generated: October 25, 2026

Methyl thiocyanate → 4-(4-n-Octylphenyl)-2-cyanophenol

https://huagongshe.com/reaction/1492351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl thiocyanateHCID 11168—
ReactantSodium HydroxideHCID 14798—
ReactantBoron TrichlorideHCID 25135—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4'-Octyl-[1,1'-biphenyl]-4-olHCID 14047211—
Solvent1,2-DichloroethaneHCID 11—
Product4-(4-n-Octylphenyl)-2-cyanophenolHCID 18950119—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 2.82 g of 4-(4-n-octylphenyl) phenol in 40 ml of 1,2-dichloroethane were added under ice cooling, 6 ml of a solution of boron trichloride (2M) in 1,2-dichloroethane, and then 0.82 ml of methyl thiocyanate and 1.33 g of aluminum chloride. The mixture was stirred at room temperature until the aluminum chloride is dissolved, further stirred for 3 hours at 80° C. and cooled to room temperature. To the resulting mixture was added further 33 ml of 4N-sodium hydroxide solution. The mixture was stirred for 30 minutes at 75° to 80° C. After cooling, the reaction mixture was washed with methylene chloride. The aqueous phase was adjusted to pH2 with 6N hydrochloric acid and extracted with ether. The extract was dried and evaporated under reduced pressure to obtain crude crystals. The crystals were purified by a silica gel column chromatography to give 2.03 g of 4-(4-n-octylphenyl)-2-cyanophenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374373
Source datasetuspto-grants-1994_12
ORD IDord-a6811cdea89441968ceecba62e61f17d
Source noteuspto-grants-1994_12