HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Dimethyl 4,4a,9,9a-tetrahydro-1,3-dimethyl-3,9-methano-3H-indeno[2,1-c]pyridine-9a,10-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Dimethyl 2,6-dimethyl-4-(2-ethenylphenyl)-1,4-dihydropyridine-3,5-dicarboxylate | HCID 13449179 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Dimethyl 4,4a,9,9a-tetrahydro-1,3-dimethyl-3,9-methano-3H-indeno[2,1-c]pyridine-9a,10-dicarboxylate | HCID 13449182 | — |
Reaction Steps
Into a solution of the Compound 2b (0.3 mmol) in dry chloroform (5 ml) was bubbled anhydrous hydrogen chloride. The resulting solution was stirred for 2.5 hours at ambient temperature. The reaction mixture was diluted chloroform (10 ml) and water (5 ml) and then neutralized with concentrated aqueous ammonium hydroxide. The organic phase was separated and the aqueous phase extracted with chloroform (2×20 ml). The combined organic phases were washed with brine, dried over anhydrous sodium sulfate and filtered. The solvent was removed in vacuo and the resulting yellow oil purified by flash chromatography on silica gel eluted with hexane:diethyl ether (1:2). The β-isomer had an Rf =0.4 and the α-isomer had an Rf =0.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04587253 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-cadafddd6afd45aeab0032d647a8da92 |
| Source note | uspto-grants-1986_05 |