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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 6-(4-Formyl-2-methylphenoxy)nicotinonitrile | HCID 59730245 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-[4-(2-Methoxy-vinyl)-2-methyl-phenoxy]-nicotinonitrile | HCID 68746462 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381719B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-dd4f5b76281e490dabc519118b00bfbd |
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| Source note | uspto-grants-2008_06 |
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