HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356467Generated: October 26, 2026
Pyridine → 3-(4-Benzyloxy-phenyl)-N-methoxy-N-methyl-propionamide
https://huagongshe.com/reaction/356467
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 3-(4-Benzyloxyphenyl)propionic acid | HCID 561372 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 3-(4-Benzyloxy-phenyl)-N-methoxy-N-methyl-propionamide | HCID 18798659 | — |
Reaction Steps
3-(4-Benzyloxyphenyl) propionic acid prepared in Example S (30 g, 117 mmol) was taken up in 300 mL of thionyl chloride. The reaction was kept under reflux for 5 hours, then cooled and concentrated. The residue was dissolved in 300 mL of CH2Cl2 and treated with N,O-dimethylhydroxylamine hydrochloride (14.1 g, 146 mmol) and 60 mL of pyridine at 0° C. The reaction was stirred overnight. The reaction was quenched with dilute HCl and extracted into EtOAc, and the organic layer was washed with sodium bicarbonate solution and dilute HCl and dried. The organic layer was dried (MgSO4) and concentrated. The residue was used further as crude reaction mixture or purified by flash silica gel column chromatography, eluting with EtOAc:hexane (1:9, then switching to 2:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834506 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-2cedc33d0ff74e33835ad9a21efa296a |
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| Source note | uspto-grants-1998_11 |
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