HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutyryl chloride → 2-Bromo-4-isobutyramidothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Bromo-1,3-thiazol-4-amine--hydrogen bromide (1/1) | HCID 20294041 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Bromo-4-isobutyramidothiazole | HCID 20377172 | 20% |
Reaction Steps
A solution of isobutyryl chloride (4.15 ml, 40 mM) in pyridine (50 ml) was cooled to 0° C. and treated portionwise with 4-amino-2-bromothiazole hydrobromide (7.8 g, 30 mM). After stirring for 1 h. the reaction mixture was poured onto 20% aqueous sodium acetate solution (500 ml) and extracted with chloroform (3×200 ml). The combined organic layers were dried and the solvents removed under reduced pressure to yield an oil which eventually crystallised. Recrystallisation from 60°-80° petroleum ether gave the title compound (2 g, 20%). mp: 95° (Found: C, 34.1; H, 3.8; N, 11.3. C7H9BrN2OS requires C, 33.7; H, 3.6; N, 11.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04148904 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-8faac4e8a21c423e9422d03aed07fea3 |
| Source note | uspto-grants-1979_04 |