HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977706Generated: October 31, 2026
Phenyl cyanate → 4-(p-Chlorophenyl)-4-methyl-2-pentynenitrile
https://huagongshe.com/reaction/1977706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl cyanate | HCID 70740 | — |
| Reactant | HCID 15431059 | HCID 15431059 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-(p-Chlorophenyl)-4-methyl-2-pentynenitrile | HCID 21995534 | 81.3% |
Reaction Steps
A solution of 1,1-dibromo-3-(p-chlorophenyl)-3-methyl-1-butene (38.5 g, 0.113 mol) in tetrahydrofuran is treated with n-butyllithium (0.25 mol, 100 mL of a 2.5 M solution in hexane) under nitrogen over 45 minutes while maintaining the temperature below −65° C., stirred overnight at dry ice/acetone bath temperature, treated dropwise with a solution of phenyl cyanate (14.89 g, 0.125 mol) in tetrahydrofuran over 30 minutes at −65° C. to −70° C., allowed to warm to 10° C., and diluted with ethyl acetate and 5% sodium hydroxide solution. The resultant mixture is extracted with ethyl acetate. The organic extracts are combined, washed sequentially with 5% sodium hydroxide solution and water, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a residue. The residue is distilled to give the title product as an oil (18.7 g, bp 110-113° C./0.9 mm Hg, 80.7% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06235754B1 |
|---|
| Source dataset | uspto-grants-2001_05 |
|---|
| ORD ID | ord-c37c751d289f4dbd9cffab2a148ce3cc |
|---|
| Source note | uspto-grants-2001_05 |
|---|