HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 2-(5-Methylpyridin-2-yl)-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Methylpicolinic acid | HCID 199575 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(5-Methylpyridin-2-yl)-1,3-benzothiazole | HCID 12354112 | 88.4% |
Reaction Steps
22.5 g (0.18 mol) of o-aminothiophenol, 25 g (0.18 mol) of 5-methylpicolic acid and 100 g of polyphosphoric acid were admixed and stirred in nitrogen gas streams at 170°-200° C. and the mixture was poured in 1 l of water. The mixture was adjusted to pH 5 with an aqueous solution of sodium hydroxide and the resulting crystals were recovered by filtration, whereupon 40 g of 2-(benzothiazol-2-yl)-5methylpyridine was obtained as crude crystals. This crude product was recrystallized from ligroine. By the above procedure was obtained 36 g of the same compound as colorless flakes melting at 169.5°-170.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232010 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-a78161e6770442f0bac33bd238d93fb8 |
| Source note | uspto-grants-1980_11 |