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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443734Generated: October 27, 2026

(3,4-Dimethoxyphenyl)acetic acid → HCID 12570797, compound

https://huagongshe.com/reaction/443734

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3,4-Dimethoxyphenyl)acetic acidHCID 7139—
Reactantalpha-(1-Amino-1-methylethyl)benzenemethanolHCID 26760—
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
Reactant2-(Oxolan-2-yl)ethan-1-olHCID 11989572—
ProductHCID 12570797HCID 1257079782%

Reaction Steps

A solution of 8.3 g. (0.05 mole) of α-(1-amino-1-methylethyl)benzenemethanol, 9.8 g. (0.05 mole) of 3,4-dimethoxyphenylacetic acid and 13.6 g. (0.055 mole) of EEDQ (Aldrich Chem. Co.) in 300 ml. of tetrahydrofuran-ethanol is refluxed for 45 minutes and then allowed to stand for 20 hours at 25° C. The solution is evaporated in vacuo. The residue is taken up with 250 ml. of ethyl acetate, washed with dilute HCl, followed by washing with aqueous NaHCO3. Subsequently, the extract is washed with aqueous NaCl, dried (Na2SO4) and evaporated to dryness in vacuo. Crystallization of the residue from ether gives 14.0 g. (82% yield) of pure 2-(3,4-dimethoxyphenyl)-N-(β-hydroxy-α,α-dimethylphenethyl)acetamide, m.p. 123°-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261890
Source datasetuspto-grants-1981_04
ORD IDord-be27a9499e3c46a391df1b8fa8dbd5f3
Source noteuspto-grants-1981_04