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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300482Generated: October 30, 2026

2,3-Dihydro-1,4-benzodioxin-6-carbaldehyde → HCID 54016659, compound

https://huagongshe.com/reaction/2300482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 248127—
ReactantMethyl 3-(3-(aminomethyl)phenyl)propanoate hydrochlorideHCID 22282736—
SolventMethanolHCID 887—
ProductHCID 54016659HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-3f750ad33ef1458ab8644be0b8ba11bf
Source noteuspto-grants-2002_12