HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-Tert-butyl-2-(5-hydroxymethylbenzofuran-2-yl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Tert-butyl-2-(5-formylbenzofuran-2-yl)thiazole | HCID 19603806 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Tert-butyl-2-(5-hydroxymethylbenzofuran-2-yl)thiazole | HCID 19092753 | 100% |
Reaction Steps
To a cooled mixture of 4-tert-butyl-2-(5-formylbenzofuran-2-yl)thiazole (2.85 g) in methanol (28 ml), sodium borohydride (0.38 g) was added in small portions. After being stirred at the same temperature for 2 hours, the resulting solution was poured into ice-water. The resulting precipitates were collected by filtration and washed with water to give 4-tert-butyl-2-(5-hydroxymethylbenzofuran-2-yl)thiazole (2.87 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05296495 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-0d6b6542c7e24beeb2fbd755ab36b99f |
| Source note | uspto-grants-1994_03 |