HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48131Generated: October 25, 2026
Benzoic acid 1-cyano-3-(4-methoxyphenyl)-allyl ester → 4-(4-Methoxyphenyl)but-3-enenitrile
https://huagongshe.com/reaction/48131
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoic acid 1-cyano-3-(4-methoxyphenyl)-allyl ester | HCID 54392804 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Methoxyphenyl)but-3-enenitrile | HCID 54435199 | 57% |
Reaction Steps
Benzoic acid 1-cyano-3-(4-methoxy-phenyl)-allyl ester (15 g; ca 0.050 mol) is dissolved in 100 ml of anhydrous tetrahydrofuran. Tetrakis(triphenylphosphine)palladium (0.88 g; 0.8 mmol) and 4.8 ml of poly(methylhydrosiloxane) (ca 80 meq; Aldrich) are added, and the mixture is stirred at ca 20° C., cooling with a cold water bath. After 3 h 30 min, the mixture is concentrated by rotary evaporation, stirred with 150 ml of water to hydrolyze the siloxane. The polymer and organic materials are redissolved in CH2Cl2 and washed with saturated sodium bicarbonate to remove benzoic acid. Evaporation of the solvent and flash chromatography (150 g SiO2; hexane:ethyl acetate 80:20 v:v) affords 4.9 g (57%) of pure 4-(4-methoxy-phenyl)-but-3-enenitrile, mp 75-76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06703182B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-0ab9cabf15834044aea6d28280ea2ec8 |
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| Source note | uspto-grants-2004_03 |
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