HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl phosphite → 2-(Benzothiazol-2-yl)-5-dimethoxyphosphinylmethylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Reactant | 2-(Benzothiazol-2-yl)-5-bromomethylpyridine | HCID 23332522 | — |
| Product | 2-(Benzothiazol-2-yl)-5-dimethoxyphosphinylmethylpyridine | HCID 23332524 | 70% |
Reaction Steps
1.5 g (0.0049 mol) of 2-(benzothiazol-2-yl)-5-bromomethylpyridine was reacted with 3 ml of trimethyl phosphite in nitrogen gas streams at 130°-160° C. for 15 minutes. The reaction mixture was allowed to cool down to room temperature and the resulting crystals were recrystallized from ethyl acetate. By the above procedure was obtained 1.1 g (70%) of 2-(benzothiazol-2-yl)-5-dimethoxyphosphinylmethylpyridine as colorless needles, m.p. 151.5°-152.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232010 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-85607935791142ba8bc37cafdb020993 |
| Source note | uspto-grants-1980_11 |