HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3,4-Trimethoxybenzaldehyde → HCID 11448955, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3,4-Trimethoxybenzaldehyde | HCID 75006 | — |
| Reactant | (3,4-Dimethoxybenzylidene)-(2,2-dimethoxyethyl)-amine | HCID 11253799 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 11448955 | HCID 11448955 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781445B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-3e0e75b21f4345d5b526dbae43b37953 |
| Source note | uspto-grants-2010_08 |