HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 15147735, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2S)-1-Methyl-2-pyrrolidinemethanol | HCID 643492 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 15147735 | HCID 15147735 | — |
Reaction Steps
(S)-1-methyl-2-pyrrolidinemethanol (5.10 g, 50 mmol, Aldrich Chemical Co.) was dissolved in 50 mL of CHCl3, then 5.25 mL of allyl bromide and 8.34 mL of triethylamine were added. The reaction mixture was stirred at room temperature for 2 hours, then the volatiles were removed under reduced pressure. The residue was purified by chromatography on silica gel to give 6.3 g of the title product. MS (DCI/NH3) m/e: 142 (M+H)+. 1H NMR (CDCI3, 300 MHz) δ: 6.05-5.90 (m, 1H), 5.33-5.17 (m, 2H), 3.77-3.68 (m, 1H), 3.58-3.47 (m, 2H), 3.32-3.20 (m, 1H), 3.16-3.05 (m, 1H), 2.90-2.78 (m, 1H), 2.53-2.40 (m, 1H), 2.02-1.73 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05914328 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-c1556efea887430186b6b8f1fd496035 |
| Source note | uspto-grants-1999_06 |