HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474556Generated: October 30, 2026
Carbon Tetrachloride → HCID 86658928, compound
https://huagongshe.com/reaction/1474556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 86658929 | HCID 86658929 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86658928 | HCID 86658928 | 58% |
Reaction Steps
Triphenyl phosphine (2.47 g, 9.8 mmol) and carbon tetrachloride (1.4 g, 9.1 mmol) were added to a THF solution (30 ml) of 5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydro-quinoline-2-carboxy-(2-hydroxyethyl)amide (3.0 g, 7.24 mmol) and heated under reflux for 2 hours. The mixture was cooled to room temperature, and water was then added thereto, followed by extraction with dichloromethane. The thus-obtained organic layer was washed with water, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified using silica gel column chromatography (dichloromethane:methanol=100:0→20:1). The purified material was concentrated to dryness under reduced pressure, giving a white powder of 5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydroquinoline-2-carboxy-(2-chloroethyl)amide (1.8 g, yield: 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09018229B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-81c81c1612ef424b96803c643bc6c742 |
|---|
| Source note | uspto-grants-2015_04 |
|---|