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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3,4-Dimethoxyphenyl)acetic acid | HCID 7139 | — |
| Reactant | 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline | HCID 27833 | — |
| Reactant | HCID 12570782 | HCID 12570782 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12570798 | HCID 12570798 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261890 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-2539738979ac40b594c18c073765a0bf |
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| Source note | uspto-grants-1981_04 |
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