HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 18469926, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Methylhomopiperazine | HCID 228349 | — |
| Reactant | HCID 18469942 | HCID 18469942 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18469926 | HCID 18469926 | — |
Reaction Steps
N-Methylhomopiperazine (2.31 g; 20.2 mmol) and potassium iodide (0.35 g; 2.2 mmol) in DMF (13 ml) were reacted with 1-chloro-6-bromo-1,2,3,4-tetrahydronapthalene (2.48 g; 10.1 mmol) in DMF (8 ml) as in Example 15. The yellow oil was kugelrohr distilled to give the title compound, 1.47 g, bp (air bath temperature) 152°-165° C. at 0.10 torr; 1H NMR (300 MHz, CDCl3) δ 2.38 (s, 3H, NCH3), 3.81 (t, 1H, ArCHN), 7.19 (s, 1H), 7.25 (d, 1H), 7.64 (d, 1H). Anal: Calcd. for C16H23BrN2: C, 59.45; H, 7.17; N, 8.67. Found: C, 59.40; H, 7.02; N, 8.30. 1-Chloro-6-bromo-1,2,3,4-tetrahydronaphthalene was prepared as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06417183B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-92d17fd6d6714d569ac46cd7d108cf03 |
| Source note | uspto-grants-2002_07 |