HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Terephthalaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1,4-Benzenedimethanol | HCID 11506 | — |
| Reactant | Sodium Bromate | HCID 23668195 | — |
| Solvent | Water | HCID 962 | — |
| Product | Terephthalaldehyde | HCID 12173 | — |
Reaction Steps
In the same manner as in Example 3, the operation was conducted, except that 0.55 g (4 mmols) of p-xylylene glycol was used in place of m-methoxybenzyl alcohol and 1 ml (17.4 mmols) of acetic acid was used in place of 2 ml of acetic acid, and also 1 ml of water and 0.4 g (2.7 mmols) of sodium bromate were used. With respect to the components in the reaction solution, the intended p-phthalaldehyde was produced in an area ratio, as determined by gas chromatography, of 56.0% and p-hydroxymethylbenzaldehyde as a product at the intermediate stage (compound in which only one among two hydroxymethyl groups in a molecule of the raw material was replaced by a formyl group) was produced in an area ratio of 28.6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07342138B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-37a199fd6c6f4ed49d5a51d6e8cfa8ac |
| Source note | uspto-grants-2008_03 |