HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-(4-Phenylbenzoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Phenylbenzoyl chloride | HCID 84151 | — |
| Reactant | 4,5,6,7-Tetrahydrofuro[3,2-c]pyridine hydrochloride | HCID 19599941 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(4-Phenylbenzoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridine | HCID 19600106 | — |
Reaction Steps
To a solution of 0.160 g (1.000 mmol) of 4,5,6,7-tetrahydrofuro[3,2-c]pyridine hydrochloride and 0.55 ml (4.0 mmol) of triethylamine in 30 ml of dichloromethane, 0.26 g (1.2 mmol) of 4-biphenylcarbonyl chloride was added under ice-cooling, followed by overnight stirring at room temperature. This solution was poured into water and extracted with dichloromethane 2 times. The combined organic layer was washed with water and dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=4/1) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998433 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-80d5d21f1ad0410d834bca13cd2a4399 |
| Source note | uspto-grants-1999_12 |