HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 178447911, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | chloroform KOH | HCID 19913595 | — |
| Reactant | HCID 178447901 | HCID 178447901 | — |
| Reactant | HCID 178447909 | HCID 178447909 | — |
| Product | HCID 178447911 | HCID 178447911 | — |
Reaction Steps
18 g of SOCl2 is added, at 80°, to a suspension of 28.9 g of 2-ethoxy-5-(trans-4-propyl-cyclohexyl)-benzamide [obtainable, for example, by reaction of trans-1-(4-hydroxyphenyl)-4-propyl-cyclohexane with chloroform/KOH to give 2-ethoxy-5-(trans-4-propylcyclohexyl)-benzaldehyde, oxidation to the acid, reaction with SOCl2 to give the chloride and reaction with NH3 ] in 100 ml of toluene. After the mixture has been stirred at 80° for 6 hours, cooled and poured into water, 2-ethoxy-5-(trans-4-propyl-cyclohexyl)-benzonitrile of m.p. 32° is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04478740 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-73f95f4c04d84b6a8a84c1a74d8a2353 |
| Source note | uspto-grants-1984_10 |