HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-(4-Fluorophenoxy)-alpha-cyanobenzyl alpha-cyclopropyl-4-chlorophenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-(4-Fluorophenoxy)-alpha-cyanobenzyl alcohol | HCID 10399513 | — |
| Reactant | alpha-Cyclopropyl-4-chlorophenylacetyl chloride | HCID 15083505 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(4-Fluorophenoxy)-alpha-cyanobenzyl alpha-cyclopropyl-4-chlorophenylacetate | HCID 57106850 | — |
Reaction Steps
With stirring, 1 g of pyridine in 3 ml of toluene and 2.3 g of α-cyclopropyl-4-chlorophenylacetyl chloride in 3 ml of toluene are added successively at 0° to 10° C. to a solution of 2.43 g of 3-(4-fluorophenoxy)-α-cyanobenzyl alcohol in 20 ml of toluene. After stirring for 10 hours at room temperature, the reaction mixture is washed with water, 2 N hydrochloric acid and 3% sodium bicarbonate solution. The organic layer is dried over sodium sulfate and the toluene is distilled off, affording the compound of the formula ##STR4## with a refractive index of nD20 =1.5880.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04264624 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-1c2ed2ec9e014e41813aafee7645fe09 |
| Source note | uspto-grants-1981_04 |