HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736855Generated: October 25, 2026
Triethylamine → 3-(4-Methoxyphenyl)propanamide
https://huagongshe.com/reaction/736855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | p-Methoxyphenylpropionic acid | HCID 257576 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Methoxyphenyl)propanamide | HCID 697955 | 95.9% |
Reaction Steps
(4-methoxyphenyl)propionic acid (20.0 mg, 0.11 mmol) prepared in Reference Synthetic Example 2 was dissolved in tetrahydrofuran (500 μl) in nitrogen atmosphere, and triethylamine (17 μl, 0.12 mmol) and ethyl chloroformate (11 μl, 0.12 mmol) were dropwise added under cooling with ice, followed by stirring for 15 minutes. A 28% ammonia aqueous solution was dropwise added, followed by stirring for 5 minutes, and the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:2 to 1:2) to give the desired compound 3-(4-methoxyphenyl)propionic acid amide (18.9 mg, 95%) as colorless needle crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07595415B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-a9e2fae14fb341a5a6aff73b11865638 |
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| Source note | uspto-grants-2009_09 |
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