HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → [6-(1H-Imidazol-1-yl)pyridin-3-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | methyl 6-(1H-imidazol-1-yl)nicotinate | HCID 4315458 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | [6-(1H-Imidazol-1-yl)pyridin-3-yl]methanol | HCID 14207630 | — |
Reaction Steps
NaBH4 (37.82 g) is added portionwise to a suspension of the imidazolyl ester of Step 2. above (9.98 g) in methanol at about 0.° C. The reaction mixture is heated to reflux for 71/2 hours, allowed to cool and stand 15 hours. Water (75 ml) is added, and the quenched reaction mixture evaporated, affording a solid residue which is suspended in water, extracted with chloroform dried over Na2SO4, filtered and evaporated, recrystallized (CHCl3), affording the desired product as a white solid. M.P.=128.5°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04954494 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-7e8ddf07c3a64967b0a43b4e4f2eeb12 |
| Source note | uspto-grants-1990_09 |