HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3,4-Trimethoxybenzaldehyde → 6,7,8-Trimethoxynaphthalene-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3,4-Trimethoxybenzaldehyde | HCID 75006 | — |
| Reactant | 4,4-Dimethoxybutyronitrile | HCID 84558 | — |
| Product | 6,7,8-Trimethoxynaphthalene-2-carbonitrile | HCID 21891620 | — |
Reaction Steps
2,3,4-Trimethoxybenzaldehyde (9.8 g) and 3-cyanopropionaldehyde dimethylacetal (6.35 mL) were treated under the same conditions as in Preparation Example 1 to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135473B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-8773f843b97e4634a9821e7af0e2fd66 |
| Source note | uspto-grants-2006_11 |