HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 14418810, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 22051939 | HCID 22051939 | — |
| Reactant | HCID 23035827 | HCID 23035827 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14418810 | HCID 14418810 | — |
Reaction Steps
4-(2-n-Nonyl-1,3,4-thiadiazole-5-yl)-benzoic acid (0.005 moles, 1.66 g) is reacted with 5 mL of thionyl chloride and heated 2 hours at the boiling point. After that, the excess thionyl chloride is distilled off in the rotary evaporator and the residue is treated with 0.006 moles (1.33 g) octyloxyphenol, dissolved in 20 mL toluene, 5 mL triethylamine and 100 mg 4-dimethylaminopyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04952699 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-e8595434f14a4ddead51b5cf5da76f84 |
| Source note | uspto-grants-1990_08 |