HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877393Generated: November 1, 2026
tert-Butyl 4-oxo-3,4-dihydroquinoline-1(2H)-carboxylate → tert-butyl 4-methylene-3,4-dihydroquinoline-1(2H)-carboxylate
https://huagongshe.com/reaction/1877393
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-oxo-3,4-dihydroquinoline-1(2H)-carboxylate | HCID 23433504 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-butyl 4-methylene-3,4-dihydroquinoline-1(2H)-carboxylate | HCID 67367966 | 73% |
Reaction Steps
A solution of methyltriphenylphosphonium bromide (1.92 g, 5.38 mmol, 1.1 equiv; [CAS RN 1779-49-3]) and potassium tert-butoxide (0.60 g, 5.38 mmol, 1.1 equiv; [CAS RN 865-47-4]) in toluene (20 mL) were heated to reflux. After 1 h, 4-oxo-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester (1.21 g, 4.89 mmol, 1.0 equiv; [CAS RN 179898-00-1]), dissolved in toluene (10 mL), was added and heating continued for one additional hour. The reaction mixture was extraction from a sat. solution of NH4Cl (100 mL) with ethyl acetate (3×50 mL) and the combined organic phases dried over MgSO4. Purification by silica column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of heptane/ethyl acetate afforded 0.87 g (73%) of the title compound as a colorless oil. MS (ISP): 246.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309734B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-adea94ad97bd4b8f8003ccbacd14bd63 |
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| Source note | uspto-grants-2012_11 |
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