HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-phenylthiazole-4-carboxylate → HCID 59455496, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-phenylthiazole-4-carboxylate | HCID 12300673 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59455496 | HCID 59455496 | 56.7% |
Reaction Steps
Prepare a cold (0° C.) solution of 5-phenylthiazole-4-carboxylic acid ethyl ester (3.0 g, 12.9 mmol) in tetrahydrofuran (150 mL). Add LiAlH4 (488 mg, 12.9 mmol). Allow the reaction to slowly warm to room temperature and stir for 3 hours. Quench with water (25 mL) and filter through Celite®. Concentrate the filtrate in vacuo to a residue. Chromatograph (silica gel, 3:7 hexane/ethyl acetate) to afford (5-phenylthiazol-4-yl)methanol (1.4 g). 1H NMR (CDCl3) δ 8.75 (s, 1H), 7.40-7.55 (m, 5H), 4.80 (d, J=4 Hz, 2H), 3.15-3.22 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07265246B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-c91c0682e7784c08987edb7521b6a972 |
| Source note | uspto-grants-2007_09 |