HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → (S)-3-(1-(p-Nitrophenoxycarbonyloxy)ethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | (S)-1-(3-Pyridyl)ethanol | HCID 10725338 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-3-(1-(p-Nitrophenoxycarbonyloxy)ethyl)pyridine | HCID 54241400 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A 534 mg (2.65 mmol) sample of p-nitrophenoxycarbonylchloride in methylene chloride was added to a solution of 74 mg (0.606 mmol) of (S)-1-(3-pyridyl)ethanol and 0.080 mL of 4-methylmorpholine in 2 mL of methylene chloride cooled in an ice bath. The mixture was stirred at 0° C. for 3.5 hours. The mixture was diluted with methylene chloride, which was washed with water, dried and concentrated. The crude product was chromatographed on silica gel, eluting with 50% and 90% ethyl acetate in hexane. The solvent was removed and the product dried to afford 0.078 g of the title compound, which was taken directly to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597926 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-a6021fc2b4db4dd8b4d99cf16fb83fd6 |
| Source note | uspto-grants-1997_01 |