HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 7a-ethynylhexahydro-1H-pyrrolizine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,2,3,5,6,7-Hexahydropyrrolizinylium perchlorate | HCID 86752340 | — |
| Reactant | HCID 178418486 | HCID 178418486 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride dihydrate | HCID 23713072 | — |
| Product | 7a-ethynylhexahydro-1H-pyrrolizine | HCID 19597695 | 71.3% |
Reaction Steps
1,2,3,5,6,7-Hexahydropyrrolizinylium perchlorate (1.0 g, 4.8 mmol) was added to a solution of 0.5M ethynylmagnesium bromide (29 mL, 14.3 mmol) in THF at room temperature. The reaction mixture was allowed to stir for 45 minutes, and 15% NaOH solution was added. The slurry was diluted with brine:water (1:1) and extracted with CH2Cl2 (3×). The organic phases were combined, dried (MgSO4), concentrated and chromatographed (silica gel; CHCl3 /MeOH, 90:10) to afford an amber oil (463 mg, 71%): 1H NMR (CDCl3, 300 MHz) δ1.75-2.06 (m, 6H), 2.14-2.23 (m, 2H), 2.33 (s, 1H), 2.53-2.62 (m, 2H), 3.22-3.28 (m, 2H); MS (Cl/NH3) m/z: 136 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05733912 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-eafa3d7b107148f580724adaf23e414c |
| Source note | uspto-grants-1998_03 |