HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 86653284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 1-formyl-4-oxo-4H-quinolizine-3-carboxylate | HCID 20634151 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86653284 | HCID 86653284 | — |
Reaction Steps
The ethyl 1-formyl-4-oxo-4H-quinolizine-3-carboxylate (5 g, 20.4 mmol) was stirred in a 2:1 dichloromethane:MeOH solution (102 mL) and cooled to 0° C. The reaction was treated with sodium borohydride (0.309 g, 8.16 mmol), warmed to ambient temperature, and stirred for 20 hours. The mixture was quenched with a 10% sodium carbonate solution, extracted with dichloromethane (3×100 mL), and partitioned between water and dichloromethane. The combined organic extracts were dried over sodium sulfate, filtered and concentrated to afford ethyl 1-(hydroxymethyl)-4-oxo-4H-quinolizine-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273737B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-c5f6df44ff1c45dea153ed329fd16e58 |
| Source note | uspto-grants-2012_09 |