HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030950Generated: October 30, 2026
Benzylamine → Hydrocinnamamide, N-benzyl-p-methoxy-
https://huagongshe.com/reaction/1030950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3-(p-Methoxyphenyl)propionic acid | HCID 95750 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Hydrocinnamamide, N-benzyl-p-methoxy- | HCID 64876 | 68.1% |
Reaction Steps
To a solution of 10.80 g (0.060 mole) of 3-(4-methoxyphenyl) propanoic acid and 6.57 g (0.065 mole of triethylamine in 25 ml dichloromethane at about 0.5° C., 6.84 g (0.063 mole) of ethyl chloroformate was added dropwise. The mixture was stirred for about 15 minutes at a temperature of about 5° to 10° C., then 6.96 g (0.065 mole) of benzylamine were added. The resulting mixture was stirred for about thirty minutes, and the solvent was evaporated. The residue was slurried in 5% aqueous sodium hydroxide. The solid was collected by filtration and rinsed with water until neutral. The washing process was repeated using 5% hydrochloric acid. The residue was dried under vacuum to give 11.0 g of the above-identified product, melting point 92°-94° C., which was suitable for use in step (b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05108363 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-cbc63581a92441fcb72cd35e029f3584 |
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| Source note | uspto-grants-1992_04 |
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