HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydro-1,4-benzodioxin-6-carbaldehyde → HCID 54016659, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydro-1,4-benzodioxin-6-carbaldehyde | HCID 248127 | — |
| Reactant | Methyl 3-(3-(aminomethyl)phenyl)propanoate hydrochloride | HCID 22282736 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54016659 | HCID 54016659 | — |
Reaction Steps
The title compound of Step A was prepared from 3-(3-aminomethyl-phenyl)-propionic acid methy ester hydrochloride salt, of Preparation 44, and 2,3- dihydro-benzo[1,4]-dioxine-6-carbaldehyde using the method described in Example 1, Step A except the imine was formed in MeOH at reflux over 3 h. 1H NMR (400 MHz, CDCl3) δ 7.26-7.16 (m, 3H), 7.07 (d, 1H), 6.85-6.78 (m, 3H), 4.24 (s, 4H), 3.75 (s, 2H), 3.68 (s, 2H), 3.66 (s, 3H), 2.94 (t, 2H), 2.62 (t, 2H); MS 342 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498172B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-3f750ad33ef1458ab8644be0b8ba11bf |
| Source note | uspto-grants-2002_12 |