HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 5-(bromomethyl)thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Methyl-1,3-thiazole-4-carboxylic acid | HCID 14109320 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 5-(bromomethyl)thiazole-4-carboxylate | HCID 66601492 | — |
Reaction Steps
To a mixture of 5-methylthiazole-4-carboxylic acid 3a (0.50 g, 3.49 mmol) in MeOH (15 mL) at 0° C. was added SOCl2 (0.51 mL, 6.99 mmol). The reaction was warmed up to room temperature and then heated to reflux for 8 h. The reaction mixture was cooled to room temperature and concentrated. The residue was dissolved in CH2Cl2 and washed with aq. NaHCO3. The organic solution was dried over Na2SO4 and concentrated. A portion of the resulting mixture (250 mg, 1.59 mmol) was heated to reflux in CCl4 (15 mL) with NBS (311 mg, 1.75 mmol) and benzoyl peroxide (38.5 mg, 0.159 mmol) for 3 h. The reaction mixture was concentrated and purification by flash column chromatography (silica gel, 30% EtOAc/heptane) gave compound 3b (250 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759533B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-c2ae47cd7eab44fdbe243cffc793f3cf |
| Source note | uspto-grants-2014_06 |