HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496655Generated: October 31, 2026
Bromide ion → 3-(allyloxy)-N-methoxy-N-methylbenzamide
https://huagongshe.com/reaction/496655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | 3-hydroxy-N-methoxy-N-methylbenzamide | HCID 21865376 | — |
| Product | 3-(allyloxy)-N-methoxy-N-methylbenzamide | HCID 22322057 | — |
Reaction Steps
To a solution of 10.8 g (59.6 mmol) B5 and 5.42 ml (71.5 mmol) allylic bromide in 300 ml 2-butanone 41.1 g (298 mmol) potassium carbonate were added. After stirring at 60° C. for 15 hours the solvent was distilled off and the residue partitionated between ethyl acetate and water. The organic layer was dried over sodium sulfate and the solvent removed in vacuo. Yield: 12.1 g (92%) B10 as a yellowish oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06946471B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-481df5f565554f3e8ef5affbce15ebf1 |
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| Source note | uspto-grants-2005_09 |
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