HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(5-Methyl-2-phenyl-4-thiazolylmethoxy)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(5-Methyl-2-phenyl-4-thiazolylmethoxy)benzaldehyde | HCID 23025085 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(5-Methyl-2-phenyl-4-thiazolylmethoxy)benzyl alcohol | HCID 68886269 | 94.1% |
Reaction Steps
To a mixture of 4-[(5-methyl-2-phenyl-4-thiazolyl)methoxy]benzaldehyde (6.00 g), tetrahydrofuran (30 ml) and methanol (20 mL) was added sodium borohydride (0.38 g) under ice-cooling, and the mixture was stirred at room temperature for 30 min. Dilute hydrochloric acid and water were added to acidify the reaction mixture, and the precipitated solid was collected by filtration, and dried with air to give crystals (5.68 g, 94%) of [4-[(5-methyl-2-phenyl-4-thiazolyl)methoxy]phenyl]methanol. Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 94-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238716B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-242f924ace3d4ade805bb10fba084c43 |
| Source note | uspto-grants-2007_07 |