HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 13472773, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | HCID 13472782 | HCID 13472782 | — |
| Product | HCID 13472773 | HCID 13472773 | — |
Reaction Steps
By following the two step procedure of example 4, but replacing methyl iodide with an equivalent amount of ethyl iodide, 2-ethyl-4,5-dimethoxy-1,2,3,7,8,12b-hexahydrobenzo[6,7]cyclohepta[1,2,3-de]isoquinoline; mp 105°-106° C.; NMR (CDCl3) δ 1.29 (t, J=7 Hz, 3H), 2.65 (t,J=7 Hz, 2H), 3.69 & 3.73 (2s, 6H), 4.55 (t, J=4 Hz, 1H), 6.41 (s, 1H), 7.10 (m, 3H), 7.35 (m, 1H); Anal Calcd for C21H25NO2 : C, 77.98% H, 7.79% N, 4.33%; Found: C, 78.17% H, 8.21% N, 4.33%, was obtained via the quaternary Schiff base, 2-ethyl-4,5-dimethoxy-1,7,8,12b-tetrahydrobenzo[6,7]cyclohepta[1,2,3-de]isoquinolinium iodide, mp 179°-181° C.; NMR (CDCl3) δ 1.78 (t, 3H), 3.84 & 3.92 (2s, 6H), 5.25 (m, 1H), 6.9-7.4 (m, 4H), 7.8 (s, 1H), 10.0 (s, 1H); IR (CHCl3) 1660 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04522946 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-270f7e0c6c634c04aeaeb25b9165e319 |
| Source note | uspto-grants-1985_06 |