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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505364Generated: November 3, 2026

2,3,4-Trimethoxybenzaldehyde → HCID 11448955, compound

https://huagongshe.com/reaction/505364

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-TrimethoxybenzaldehydeHCID 75006—
Reactant(3,4-Dimethoxybenzylidene)-(2,2-dimethoxyethyl)-amineHCID 11253799—
SolventBenzeneHCID 241—
ProductHCID 11448955HCID 11448955100%

Reaction Steps

2,3,4-Trimethoxybenzaldehyde (10e, 11.48 g, 0.05851 mol) was dissolved in benzene (200 mL) and aminoacetaldehydedimethylacetal (10.0 mL, 9.75 g, 0.0927 mol) was added. The same procedure was applied as for 11a. The product was isolated as a clear light yellow oil (16.58 g, 100%), bp 153-155° C. (0.45 mm Hg). 1H NMR (300 MHz CDCl3) 8.49 (s, 1H), 7.64 (d, J=8.7 Hz, 1H), 6.65 (d, J=8.7 Hz, 1H), 4.61 (t, J=5.4 Hz, 1H), 3.88 (s, 3H), 3.84 (s, 3H), 3.82 (s, 3H), 3.71 (d, J=5.4 Hz, 2H), 3.36 (s, 6H); low resolution ESIMS m/z (rel intensity) 284 (MH+, 100), 252 (45). Anal. Calcd for C14H21NO5: C, 59.35; H, 7.47; N, 4.94. Found: C, 59.67; H, 7.55; N, 4.88.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781445B2
Source datasetuspto-grants-2010_08
ORD IDord-3e0e75b21f4345d5b526dbae43b37953
Source noteuspto-grants-2010_08