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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043676Generated: October 31, 2026

2-Methylbenzoic acid → 6-(2-Methoxy-4-methoxymethoxyphenyl)-5-(4-methylbenzoyloxymethyl)-2,2,4-trimethyl-1,2-dihydroquinoline

https://huagongshe.com/reaction/1043676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzoic acidHCID 8373—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant5-Hydroxymethyl-6-(2-methoxy-4-methoxymethoxyphenyl)-2,2,4-trimethyl-1,2-dihydroquinolineHCID 57990585—
SolventBenzeneHCID 241—
SolventHexaneHCID 8058—
Product6-(2-Methoxy-4-methoxymethoxyphenyl)-5-(4-methylbenzoyloxymethyl)-2,2,4-trimethyl-1,2-dihydroquinolineHCID 5799058373.2%

Reaction Steps

5-Hydroxymethyl-6-(2-methoxy-4-methoxymethoxyphenyl)-2,2,4-trimethyl-1,2-dihydroquinoline (Reference Compound No. 1, 1.00 g, 2.71 mmol), 2-methylbenzoic acid (739 mg, 5.43 mmol), tri-n-butylphosphine (1.35 mL, 5.40 mmol), and 1,1′-(azodicarbonyl)dipiperidine (1.37 g, 5.43 mmol) were dissolved in anhydrous benzene (30 mL), and then the mixture was stirred under argon atmosphere at room temperature overnight. Hexane (30 mL) was added to the reaction mixture, and then the unsoluble materials were filtered out. The filtrate was concentrated under reduced pressure, and then the residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (967 mg) as a colorless amorphous product. (Yield 73%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563551B2
Source datasetuspto-grants-2013_10
ORD IDord-c7da24d070c544b286c32d9c127d467c
Source noteuspto-grants-2013_10