HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 3-(Cyclopentyloxy)-4-methoxyphenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-(Chloromethyl)-2-(cyclopentyloxy)-1-methoxybenzene | HCID 10900766 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Cyclopentyloxy)-4-methoxyphenylacetonitrile | HCID 10728228 | 96.2% |
Reaction Steps
A mixture of 3-cyclopentyloxy-4-methoxybenzyl chloride (119 grams, 0.49 mol), 120 milliliters of methylene chloride, KCN (70.7 grams, 1.09 mol), benzyltriethylammonium chloride (35 grams, 0.015 mol) and water (120 milliliters) was stirred vigorously at room temperature for 48 hours. The reaction mixture was diluted with. methylene chloride and the layers were separated. The methylene chloride solution was extracted several times with water and evaporated to yield 3-cyclopentyloxy-4-methoxyphenylacetonitrile (109 grams, 95%) for the subsequent transformation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05889014 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-30df6b9f683642bca49ccc8263a0a1f8 |
| Source note | uspto-grants-1999_03 |