HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzyl-1,3-thiazole-4-carboxylic acid → (2-Benzylthiazol-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzyl-1,3-thiazole-4-carboxylic acid | HCID 1491570 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Benzylthiazol-4-yl)methanol | HCID 13102618 | — |
Reaction Steps
2-Benzyl-4-thiazolecarboxylic acid is converted to the methyl ester and the ester is reduced with lithium aluminium hydride in tetrahydrofuran to give 2-benzyl-4-hydroxymethylthiazole. Using this compound as the starting material in the procedure of Example 1 gives N-methyl-N'-[2-((2-benzyl-4-thiazolyl)methylthio)ethyl]thiourea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04151288 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-282aad152f214ccfbd5444b07794054f |
| Source note | uspto-grants-1979_04 |