HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005946Generated: October 31, 2026
Ethyl chloroformate → HCID 22675275, compound
https://huagongshe.com/reaction/1005946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178432297 | HCID 178432297 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22675275 | HCID 22675275 | — |
Reaction Steps
In tetrahydrofuran (10 ml) was suspended 60% sodium hydride (60 mg). The compound 1 (200 mg) was added to the suspension under ice cooling, and the mixture was stirred for 30 min. Further, ethyl chloroformate (200 μl) was added thereto, and the mixture was stirred for 3 hr. The reaction solution thus obtained was poured into ice water, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine and was then dried over anhydrous sodium sulfate. The solvent was then removed under the reduced pressure. The crude product was purified by chromatography on silica gel (Wako Gel C-200, elution solvent: n-hexane-ethyl acetate (3:1)) to give 2,3-dimethyl-6-t-butyl-8-fluoro-4-ethoxycarbonyl-quinoline (compound 7, 220 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06787557B2 |
|---|
| Source dataset | uspto-grants-2004_09 |
|---|
| ORD ID | ord-91f8e54cbaf24eeb9d9077a6fea3ce8e |
|---|
| Source note | uspto-grants-2004_09 |
|---|