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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220788Generated: November 1, 2026

1,2,4-Trimethylbenzene → 3,4-Dimethylbenzoic acid

https://huagongshe.com/reaction/2220788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,4-TrimethylbenzeneHCID 7247—
Reactant3,4-DimethylbenzaldehydeHCID 22278—
Reactant3,4-Dimethylbenzyl alcoholHCID 23407—
Product3,4-Dimethylbenzoic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368267B2
Source datasetuspto-grants-2008_05
ORD IDord-2f87d10f5782437c80dc87a956189339
Source noteuspto-grants-2008_05