HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → ethyl 2-[2-(4-cyanophenyl)-2-hydroxy-1-ethylthio]-3H-imidazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | ethyl 2-[2-(4-cyanophenyl)-2-oxo-ethylthio]-3H-imidazole-4-carboxylate | HCID 22612522 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | ethyl 2-[2-(4-cyanophenyl)-2-hydroxy-1-ethylthio]-3H-imidazole-4-carboxylate | HCID 22612527 | — |
Reaction Steps
The product from Step A (6.91 g, 21.9 mmol) was suspended in methanol (50 mL). Sodium borohydride (829 mg, 21.9 mmol) was added in portions at 0° C., and the suspension was stirred until it became homogeneous (1 hour). The reaction was quenched by the addition of saturated aqueous ammonium chloride until hydrogen evolution ceased. The resulting precipitate was filtered and washed with water (2×25 mL) to provide the title product as a white solid which was sufficiently pure for use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380228B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-50d741ec296b45cfbcc61b2f50b60235 |
| Source note | uspto-grants-2002_04 |