HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Diethyl-4-(3-azidopropoxy)-2,6-pyridinedicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Azidopropan-1-ol | HCID 10996974 | — |
| Reactant | Diethyl 4-bromopyridine-2,6-dicarboxylate | HCID 13794409 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl-4-(3-azidopropoxy)-2,6-pyridinedicarboxylate | HCID 22323654 | 40% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
3-Azido-1-propanol (0.266 mL, 3.64 mmol) was dissolved in DMF (5 mL) and cooled to 0° C. NaH (146 mg, 3.64 mmol) was added and the mixture was stirred for 15 minutes. Diethyl-4-bromo-2,6-pyridinedicarboxylate dissolved in DMF (5 mL) was added to the reaction mixture dropwise. The reaction was complete as indicated by TLC in 1 hour. The reaction mixture was partitioned between CH2Cl2 and water. The water was separated and extracted with CH2Cl2. The CH2Cl2 layers were combined, dried (MgSO4) and concentrated to an oil. The oil was purified by silica gel flash column chromatography to give a yield of 40% of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800444B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-4aaa52ed25f447a8b5acc259498403ac |
| Source note | uspto-grants-2004_10 |