HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 178469470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178469469 | HCID 178469469 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178469470 | HCID 178469470 | — |
Reaction Steps
To a suspension of 6 g of ethyl 4-hydroxy-6-oxo-5,6,7,8-tetrahydroquinoline-3-carboxylate in 200 mL of ethanol, 1.92 g of NaBH4 is added in small portions under ice-cooling and stirring. The reaction mixture is then stirred at room temperature for 6 hours and evaporated to dryness. The residue is taken up in CHCl3, washed successively with 6N NH4OH, and sat. aq. NaCl, dried (MgSO4) and evaporated dryness obtaining ethyl 4,6-dihydroxy-5,6,7,8-tetrahydroquinoline-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04740512 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-e67b9a44fa6b4818a811ea4b897cba30 |
| Source note | uspto-grants-1988_04 |