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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677235Generated: November 1, 2026

Hydrochloric Acid → 4,5-Dimethoxy-2-(1-methyl-2-phenyl-ethyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/1677235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant2-[4,5-Dimethoxy-2-(1-methyl-2-phenyl-ethyl)-phenyl]-3,4,4-trimethyl-4,5-dihydro-oxazolium iodideHCID 67053436—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
Product4,5-Dimethoxy-2-(1-methyl-2-phenyl-ethyl)-benzoic acid methyl esterHCID 5959854388.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-[4,5-dimethoxy-2-(1-methyl-2-phenyl-ethyl)-phenyl]-3,4,4-trimethyl-4,5-dihydro-oxazolium iodide (5.132 g, 10.4 mmol) in 52 mL methanol was added 4 M NaOH (5.2 mL, 20.7 mmol). The solution was warmed to reflux. After 16 hours the solution was cooled to 0° C. and acidified to pH=1 with concentrated HCl. The mixture was extracted with ethyl acetate, washed with H2O and washed with brine. The combined organics were dried over Na2SO4, filtered and concentrated in vacuo to give a crude acid (3.228 g). A portion of this acid (2.919 g, 9.73 mmol) was dissolved in a mixture of 70 mL benzene and 20 mL MeOH. Trimethylsilyldiazomethane (6.3 mL, 2.0 M in hexanes) was added drop-wise. After 30 minutes the solution was concentrated in vacuo to give 4,5-dimethoxy-2-(1-methyl-2-phenyl-ethyl)-benzoic acid methyl ester as an oil (2.886 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008313B2
Source datasetuspto-grants-2011_08
ORD IDord-255a487d6d9341d886ee15692d128f40
Source noteuspto-grants-2011_08