HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389263Generated: October 29, 2026
Acetic Anhydride → N-Benzyl-N-(prop-1-en-1-yl)acetamide
https://huagongshe.com/reaction/389263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178457043 | HCID 178457043 | — |
| Product | N-Benzyl-N-(prop-1-en-1-yl)acetamide | HCID 9942349 | — |
Reaction Steps
To benzyl-prop-(E)-ylidene-amine (6.0 g, 40 mmol) in triethylamine (5.67 mL, 40 mmol) at 0° C. was slowly added acetic anhydride (3.81 mL, 40 mmol), and the reaction was stirred for 30 minutes at 0° C. and then overnight at room temperature. The mixture was concentrated, and the residue was purified by silica gel chromatography (0-25% EtOAc in hexanes) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378107B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-62296e56bb704f65856518b390e5b164 |
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| Source note | uspto-grants-2013_02 |
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