HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,4-Trimethylbenzene → 3,4-Dimethylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,4-Trimethylbenzene | HCID 7247 | — |
| Reactant | 3,4-Dimethylbenzaldehyde | HCID 22278 | — |
| Reactant | 3,4-Dimethylbenzyl alcohol | HCID 23407 | — |
| Product | 3,4-Dimethylbenzoic acid | HCID 12073 | — |
Reaction Steps
FIG. 9 demonstrates the formation of 3,4-dimethylbenzyl alcohol commenced immediately. The formation of 3,4-dimethylbenzaldehyde commenced after 2 hours. 11 hours after starting the fed-batch culture, another 1% (v/v) of pseudocumene was added. However, only some of this substrate was now converted. The end concentration of 3,4-dimethylbenzylaldehyde was 113 mM. When the biotransformation was stopped, the pseudocumene and 3,4-dimethylbenzyl alcohol concentrations were 65 mM. Virtually no 3,4-dimethylbenzoic acid was produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368267B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-2f87d10f5782437c80dc87a956189339 |
| Source note | uspto-grants-2008_05 |