HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → ethyl 3,4-dihydro-2H-pyrano[2,3-b]indolizine-10-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,2-Di-[(ethoxycarbonyl)methyl]pyridinium bromide | HCID 21467252 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | ethyl 3,4-dihydro-2H-pyrano[2,3-b]indolizine-10-carboxylate | HCID 21467249 | — |
Reaction Steps
A solution of 1,2-di-[(ethoxycarbonyl)methyl]pyridinium bromide (1.5 g, 0.0045 mole) and 1,3-dibromopropane (0.45 ml, 0.0045 mole) in ethanol (10 ml) was added over 5 minutes to a stirred solution of potassium hydroxide (0.75 g, 0.0134 mole) in ethanol (15 ml) at 5° C. The mixture was then allowed to warm upto room temperature and stir for 20 h. The reaction mixture was diluted with water (150 ml) and extracted with ethyl acetate (2×100 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave a brown oil. This was chromatographed on silica gel eluting with ether to afford the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05696129 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-e9e59f44f0d042cb8141c696d02a6c4e |
| Source note | uspto-grants-1997_12 |