HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288626Generated: November 3, 2026
Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester → Acrolein
https://huagongshe.com/reaction/1288626
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Acrolein | HCID 7847 | — |
| Product | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
Reaction Steps
Another embodiment of the invention utilizing the same amine groups in similar manner is the addition of one or more amine of Group A to a CAA having a high (>2,000 ppm) level of acetic acid. This high acetic acid-containing CAA feed stream may be fed to an acetic add distillation column, that is, a distillation column used for effectively reducing, by its distillation, acetic acid from the CAA. Distillation of the Group A-treated CAA yields a low acrolein (also now low acetic add) CAA. (The Group A amine can be fed to the acetic acid removal column as a separate stream as the high acetic acid CAA is fed to the column.) Subsequently, the low acrolein CAA is fed to a final distillation column, i.e., a high purity acrylic acid distillation column, where the final distillation steps, previously described, are carried out.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05746892 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-7e740a55812f4c5ea46d2cbd9fad1134 |
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| Source note | uspto-grants-1998_05 |
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