HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Phenylthiazole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl 4-phenyl-1,3-thiazole-2-carboxylate | HCID 24730326 | — |
| Reactant | HCID 86597229 | HCID 86597229 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Phenylthiazole-2-carboxylic acid | HCID 3878539 | 54% |
Reaction Steps
4-Phenyl-thiazole-2-carboxylic acid ethyl ester, commercially available from Pharma Core, (1.0 g, 4.28 mmol) in a mixture solution of tetrahydrofuran, methanol and water (3:1:1, 10 mL) was treated with lithium hydroxide monohydride (514 mg, 12.8 mmol) at room temperature for three hours. After the reaction was complete, solvent was evaporated. To the residue, water was added, and pH of the resulting solution was adjusted to ˜1-2 by addition of dilute hydrochloride acid (1N). The white precipitation was collected by centrifugation and further washed with water to give 4-phenyl-thiazole-2-carboxylic acid (473 mg, 54%). LCMS calcd for C10H7NO2S (m/e) 205, obsd 206 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714126B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-2ebee532f3004a07ad165fa6ce91dc9d |
| Source note | uspto-grants-2010_05 |