HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211232Generated: October 30, 2026
4-Cyanophenol → 4-[(2-Methylbut-3-yn-2-yl)oxy]benzonitrile
https://huagongshe.com/reaction/2211232
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | Acetic acid, trifluoro-, 1,1-dimethyl-2-propynyl ester | HCID 11830027 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[(2-Methylbut-3-yn-2-yl)oxy]benzonitrile | HCID 2779072 | — |
Reaction Steps
The 1,1-dimethyl-2-propynyl trifluoroacetate solution, maintained at 0° C., was added to the 4-cyanophenol solution over a 35 minute period while keeping the temperature at ~0° C. The resulting mixture was stirred at ~0° C. (ice bath). After stirring for 90 minutes, water (10 mL) was added and the resulting mixture was concentrated at reduced pressure. The residue was partitioned between water (50 mL) and toluene (300 mL). The organic fraction was washed with 1N HCl (3×50 mL), 1N NaOH (2×50 mL), 1N NaHCO3, and brine. After drying (magnesium sulfate), the solvent was removed at reduced pressure to give crude title compound as a yellow oil. Distillation of the crude material (bulb to bulb) afforded the title compound as a colorless, low melting solid (8.93 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05463059 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-627fbe6701bd499a8d4d5943c117a551 |
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| Source note | uspto-grants-1995_10 |
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