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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248178Generated: October 30, 2026

Methyl iodide → HCID 13472773, compound

https://huagongshe.com/reaction/1248178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantIodoethaneHCID 6340—
ReactantHCID 13472782HCID 13472782—
ProductHCID 13472773HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522946
Source datasetuspto-grants-1985_06
ORD IDord-270f7e0c6c634c04aeaeb25b9165e319
Source noteuspto-grants-1985_06