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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260807Generated: October 31, 2026

3-Methoxy-2-MethylBenzoic Acid → Methoxyfenozide

https://huagongshe.com/reaction/260807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-2-MethylBenzoic AcidHCID 7021483—
ReactantN-tert-Butyl-3,5-dimethylbenzohydrazideHCID 10878689—
SolventDichloromethaneHCID 6344—
SolventThionyl ChlorideHCID 24386—
ProductMethoxyfenozideHCID 10501057%

Reaction Steps

A solution of 3-methoxy-2-methylbenzoic acid (1.5 g, 0.01 mole) in thionyl chloride (10 mL.) was refluxed for 45 minutes and then stripped under reduced pressure. The residue was dissolved in methylene chloride (50 mL) and added dropwise with cooling at 0° C. to a solution of N-(3,5-dimethylbenzoyl)-N-tert-butylhydrazine (4.4 g. 0.02 mole) in methylene chloride (50 mL). Following the addition, the solution was stirred overnight at room temperature and filtered. The filter-cake was washed extensively with water and ether, and then dried in vacuo to give 2.1 g of N-(3-methoxy-2-methylbenzoyl)-N'-(3,5-dimethylbenzoyl)-N'-tert-butylhydrazine, melting at 204°-204.5° C. 1H-NMR δppm 1.50 (s, 9H, tert-Bu), 1.63 (s, 3H, Ar--CH3), 2.25 (s, 6H, di--CH3) 3.75 (s, 3H, OCH3), 6.26 (d, 1H, Ar), 6.93-7.20 (m, 5H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05530028
Source datasetuspto-grants-1996_06
ORD IDord-5e034e0614824442aac77f969354f862
Source noteuspto-grants-1996_06