Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443735Generated: October 29, 2026

(3,4-Dimethoxyphenyl)acetic acid → HCID 12570798, compound

https://huagongshe.com/reaction/443735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3,4-Dimethoxyphenyl)acetic acidHCID 7139—
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
ReactantHCID 12570782HCID 12570782—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12570798HCID 1257079872%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 50 g. (0.26 mole) of 3,4-dimethoxyphenylacetic acid, 68 g. (0.28 mole) of EEDQ and 50 g. (0.26 mole) of α-(1-amino-1-methylethyl)-3-methoxybenzenemethanol in 450 ml. tetrahydrofuran are stirred for three days at 25° C., and then heated for 5 hours at 65° C. Tetrahydrofuran is evaporated in vacuo, and the residue is taken up with ice and 10% aqueous H2SO4 solution to pH 2. The amide is extracted twice with 500 ml. ethyl acetate. The combined organic extracts are washed with 500 ml. dilute aqueous NH4OH solution, dried (Na2SO4) and evaporated to dryness in vacuo. The residual oil is dissolved in hot diethyl ether from which it crystallizes to give 72.0 g. of impure product. Recrystallization from diethyl ether gives 70 g. (72% yield) of N-(β-hydroxy-3-methoxy-α,α-dimethylphenethyl)-3,4-dimethoxybenzeneacetamide as white crystals of analytical purity, m.p. 137°-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261890
Source datasetuspto-grants-1981_04
ORD IDord-2539738979ac40b594c18c073765a0bf
Source noteuspto-grants-1981_04