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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18668Generated: October 25, 2026

Potassium Carbonate → 2-(4-Methoxy-2-propan-2-ylphenoxy)acetonitrile

https://huagongshe.com/reaction/18668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAcetonitrile, 2-(((4-methylphenyl)sulfonyl)oxy)-HCID 84525—
Reactant4-Methoxy-2-(propan-2-yl)phenolHCID 18364997—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-(4-Methoxy-2-propan-2-ylphenoxy)acetonitrileHCID 25241771—

Reaction Steps

A stirred slurry of toluene-4-sulfonic acid cyanomethyl ester (13.0 kg), potassium carbonate (13.0 kg) and 2-isopropyl-4-methoxyphenol (9.57 Kg) in 79.7 kg of 2-butanone was heated to 55-60 degrees C. for 4 days, then heated to relux for 18 hours. The resultant slurry was cooled and filtered to remove solids. The filtrate was concentrated under reduced pressure and the residue was redissolved in toluene. The toluene solution was extracted with 1N KOH, and the organic phase was concentrated by distillation to give 20.6 g of a 1:1 (by weight) solution of (2-Isopropyl-4-methoxy-phenoxy)-acetonitrile in toluene, which was used directly in the next step. A anliquot (96.7 g) of this solution was concentrated to dryness to give 50.9 g of crude (2-Isopropyl-4-methoxy-phenoxy)-acetonitrile, projecting to a yield of 10.9 kg in the bulk solution: MS (M+H)=206; 1H nmr (CDCl3) delta: 1.25 (d, J=6.9 Hz), 3.31 (septet, 1H, J=6.9 Hz), 3.82 (s, 3H), 4.76 (s, 2H), 6.73 (dd. 1H, J=8.8 Hz, 3.1 Hz), 6.87 (d, 1H, J=3.1 Hz), 6.91 (d, 1H, J=8.8 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741484B2
Source datasetuspto-grants-2010_06
ORD IDord-cf9b8be9f1a34379a13bab8f30306493
Source noteuspto-grants-2010_06