HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 18700234, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | HCID 10330521 | HCID 10330521 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | HCID 18700234 | HCID 18700234 | — |
Reaction Steps
A solution of 5-methyl-spiro[isobenzofuran-1(3H),4'-piperidine] (4 g), 1,6-dibromohexane (2.2 g), finely powdered potassium carbonate (2.7 g) and a crystal of potassium iodide in MIBK (150 ml) was refluxed for 4 h. Inorganic salts were filtered off and MIBK evaporated. Column chromatography on silica gel (eluted with ethyl acetate/ethanol/triethylamine 75:25:4) gave the pure title compound 11a. Yield 1.0 g. Mp 113°-116° C. (recrystallized from 2-propyl ether). 1H NMR (CDCl3) δ 1.30-1.45 (m, 4 H), 1.50-1.65 (m, 4 H), 1.80 (d, 4 H), 2.00 (dt, 4 H), 2.35 (s, 6 H), 2.45-2.50 (m, 8 H), 2.85 (broad d, 4 H), 5.05 (s, 4 H), 6.95-7.10 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05837707 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-fbee1d83560d4ad2a2b6763d2d36dcff |
| Source note | uspto-grants-1998_11 |