HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl chloroformate → 5-n-Butoxycarbonylfuro[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl chloroformate | HCID 61140 | — |
| Reactant | 3-Methylfuran-2-carbaldehyde-n-phenylimine | HCID 9815443 | — |
| Reactant | n-Butyl cyanoformate | HCID 13809822 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 5-n-Butoxycarbonylfuro[2,3-c]pyridine | HCID 18324190 | 45.8% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
n-Butyl cyanoformate(13.7 g, 0.108 mol) and 3-methylfuran-2-carbaldehyde-N-phenylimine(5.0 g, 27.0 mmol) were mixed at room temperature in xylene (25 mL) then heated to reflux at 120 to 140° C. with stirring. A xylene (15 mL) solution of 7.40 g (54.2 mol) of n-butyl chloroformate was added dropwise for an hour to the resulting mixture. After all the solution had been added, the reaction mixture was heated to reflux for 2 hours, it was allowed to cool to room temperature, and the solvent was distilled off to give 7.10 g of crude product. This product was purified by column chromatography on silica gel, giving 2.71 g (45.8% yield) of 5-n-butoxycarbonylfuro[2,3-c]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06111111 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-0d36bff69522468c8ebaccdf6f518f6b |
| Source note | uspto-grants-2000_08 |