HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzaldehyde → 2-(4-Methoxyphenyl)-4,4,5,5-tetramethylimidazolidine-1,3-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | 2,3-Butanediamine, N,N'-dihydroxy-2,3-dimethyl- | HCID 84402 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-Methoxyphenyl)-4,4,5,5-tetramethylimidazolidine-1,3-diol | HCID 59155377 | 34% |
Reaction Steps
A solution of 2,3-bis(hydroxylamino)-2,3-dimethylbutane (1.3 g, 8.8 mmol) and 4-methoxy-benzaldehyde (1.2 g, 8.8 mmol) in methanol (10 mL) was stirred at room temperature until reactants disappeared as TLC indicated. 1,3-Dihydroxy-2-(4-methoxyphenyl)-4,4,5,5-tetramethylimidazolidine was obtained by filtration, the filtrate was evaporated under reduced pressure to obtain the second crop of the title compound. The combined compound was then washed with petroleum ether and used for the next reaction (0.8 g, 34% yield). 1HNMR (400 MHz, DMSO): δ 7.63 (s, 1 H), 7.32 (d, 1 H, J=6.8), 6.87 (d, 1 H, J=5.8), 4.42 (s, 1 H), 3.72 (s, 3 H), 1.06 (s, 3 H), 1.02 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377670B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-cf814bd6504a4b24a85bc4bff699061f |
| Source note | uspto-grants-2013_02 |