HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoform → Methyl 2-bromothiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoform | HCID 5558 | — |
| Reactant | Amyl Nitrate | HCID 61250 | — |
| Reactant | Methyl 2-aminothiazole-5-carboxylate | HCID 238005 | — |
| Product | Methyl 2-bromothiazole-5-carboxylate | HCID 2773502 | — |
Reaction Steps
A mixture containing 100 g. of amyl nitrate and 600 ml. of bromoform is warmed to 70° C and then a total of 100 g. of 2-amino-5-methoxycarbonylthiazole is added portionwise with rapid stirring while maintaining the temperature at about 95°-100° C. The mixture is then stirred for an additional ten minutes at this temperature and then the bromoform is distilled off under vacuum. The residue is chromatographed on silica gel yielding 2-bromo-5-methoxycarbonylthiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04089865 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-f18bc3313aa14100afdb4d913b8f62e3 |
| Source note | uspto-grants-1978_05 |