HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 178444320, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | p-Cyanobenzyl alcohol | HCID 160549 | — |
| Reactant | HCID 178444319 | HCID 178444319 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178444320 | HCID 178444320 | — |
Reaction Steps
28.8 g of p-(trans-4-pentylcyclohexyl)-phenylacetic acid is boiled for 1 hour with 24 g of SOCl2 ; the mixture is evaporated; the crude acid chloride obtained is dissolved in 150 ml of toluene, 8 ml of pyridine and 13.3 g of p-cyanobenzyl alcohol are added; and the mixture is boiled for 2 hours. Cooling and working up in a customary manner give p-cyanobenzyl p-(trans-4-pentylcyclohexyl)-phenylacetate, m.p. 85°, c.p. 30°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04627933 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-5c254b53599b49dc89f819aa5479f99c |
| Source note | uspto-grants-1986_12 |