HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methyl-5-(2-hydroxyethyl)thiazole → 5-(2-bromoethyl)-4-methylthiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methyl-5-(2-hydroxyethyl)thiazole | HCID 1136 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2-bromoethyl)-4-methylthiazole | HCID 204187 | 62.6% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
1 g (6.98 mmol) of 2-(4-methylthiazol-5-yl)ethanol is dissolved in 15 mL of dichloromethane. The solution is cooled to 0° C. When the temperature is reached, 1.85 g (6.98 mmol) of triphenylphosphine are added, followed by portionwise addition of 1.30 g (6.98 mmol) of N-bromosuccinimide. After stirring for 2 hours at 0° C., the mixture is evaporated to dryness. The residue is purified by chromatography on silica gel (eluent: 50/50 EtOAc/heptane) to give 900 mg of 5-(2-bromoethyl)-4-methylthiazole, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321790B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-d1814a2221f348e489e0a298cd611760 |
| Source note | uspto-grants-2016_04 |