A Practical Synthesis of 3-n-Propylphenol, a Component of Tsetse Fly Attractant Blends
| dc.contributor.author | Istva´n Ujva´ry | |
| dc.contributor.author | Gyula Mikite | |
| dc.date.accessioned | 2012-11-20T14:32:47Z | |
| dc.date.accessioned | 2025-02-17T14:02:19Z | |
| dc.date.available | 2012-11-20T14:32:47Z | |
| dc.date.issued | 2012-11-20 | |
| dc.description | A practical synthesis of the tsetse fly attractant 3-n-propylphenol involves the Grignard reaction of 3-hydroxybenzaldehyde and ethylmagnesium bromide affording a benzylic alcohol-type phenol derivative that upon catalytic hydrogenation gives the title product in 75% overall yield. Selection of the right solvent mixture and temperature range for the Grignard reaction is crucial for the kilogram-scale preparation of the target compound. | en_US |
| dc.description.abstract | A practical synthesis of the tsetse fly attractant 3-n-propylphenol involves the Grignard reaction of 3-hydroxybenzaldehyde and ethylmagnesium bromide affording a benzylic alcohol-type phenol derivative that upon catalytic hydrogenation gives the title product in 75% overall yield. Selection of the right solvent mixture and temperature range for the Grignard reaction is crucial for the kilogram-scale preparation of the target compound. | en_US |
| dc.identifier.uri | https://dl.ftveti.edu.et/handle/123456789/4249 | |
| dc.language.iso | en | en_US |
| dc.subject | A Practical Synthesis of 3-n-Propylphenol, a Component of Tsetse Fly Attractant Blends | en_US |
| dc.title | A Practical Synthesis of 3-n-Propylphenol, a Component of Tsetse Fly Attractant Blends | en_US |
| dc.type | Article | en_US |
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