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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130723Generated: October 27, 2026

Toluene → 6-[4-(2-Methoxy-vinyl)-2-methyl-phenoxy]-nicotinonitrile

https://huagongshe.com/reaction/130723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant6-(4-Formyl-2-methylphenoxy)nicotinonitrileHCID 59730245—
SolventTetrahydrofuranHCID 8028—
Product6-[4-(2-Methoxy-vinyl)-2-methyl-phenoxy]-nicotinonitrileHCID 6874646276%

Reaction Conditions

Temperature0 °C

Reaction Steps

Suspend (methoxymethyl)triphenylphosphonium chloride (1.14 g, 3.34 mmol)in THF (11 mL) under N2 and cool the mixture at 0° C., add slowly 0.5M KHMDS in toluene (6.7 mL, 3.34 mmol) and stir at 0° C. for 30 min. Cool the mixture at −78° C. and add a solution of aldehyde from step 1 above (663 mg, 2.78 mmol) in THF (2 mL). Wann the mixture slowly to room temperature, and stir for 1 h. Add water and extract the aqueous layer with Et2O. Dry the organic layer over MgSO4. Eliminate the solvent and purify by flash chromatography on silica gel (eluent: gradient from EtOAc/hexane 10/90 to 20/80) to get the title compound (530 mg, 76%). Electrospray MS M+1 ion=267. 1H-NMR (CDCl3, 300 MHz, mixture of isomers): 8.47-8.45 (m, 2H), 7.92-7.86 (m, 2H), 7.50-7.45 (m, 1H), 7.15-6.93 (m, 8H), 6.14 (d, 1H, J=7.1 Hz), 5.79 (d, 1H, J=13.2 Hz), 5.20 (d, 1H, J=7.1 Hz), 3.78 (s, 3H), 3.68 (s, 3H), 2.11 (s, 3H), 2.10 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381719B2
Source datasetuspto-grants-2008_06
ORD IDord-dd4f5b76281e490dabc519118b00bfbd
Source noteuspto-grants-2008_06