HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Carboethoxy)methyliminomethyl-3,4-dimethoxybenzene → N-[1-carboethoxy-5-(3,4-dimethoxyphenyl)-5-cyano-5-(isopropyl)pentyl]iminomethyl-3,4-dimethoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Carboethoxy)methyliminomethyl-3,4-dimethoxybenzene | HCID 11299712 | — |
| Reactant | 2-(3,4-Dimethoxyphenyl)-2-isopropyl-2-(3-iodopropyl)acetonitrile | HCID 14027162 | — |
| Product | N-[1-carboethoxy-5-(3,4-dimethoxyphenyl)-5-cyano-5-(isopropyl)pentyl]iminomethyl-3,4-dimethoxybenzene | HCID 20202215 | — |
Reaction Steps
The resulting imine of formula 24 is then deprotonated using a suitable strong base, and allowed to react with a compound of formula 22 to produce a compound of formula 25 (step 2). For example, 1-(carboethoxy)methyliminomethyl-3,4-dimethoxybenzene (24) is suspended in a solution of LiNiPr2 in THF/HMPA at -78° C., then reacted with 2-(3,4-dimethoxyphenyl)-2-isopropyl-2-(3-iodopropyl)acetonitrile (22) to produce N-[1-carboethoxy-5-(3,4-dimethoxyphenyl)-5-cyano-5-(isopropyl)pentyl]iminomethyl-3,4-dimethoxybenzene (25).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04667038 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-7c71cf0b7d6a449ea49aefe9390e35f4 |
| Source note | uspto-grants-1987_05 |