HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-bromovalerate → Pentanoic acid, 5-(4-formyl-3,5-dimethoxyphenoxy)-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-bromovalerate | HCID 84580 | — |
| Reactant | 2,6-Dimethoxy-4-hydroxybenzaldehyde | HCID 529894 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Pentanoic acid, 5-(4-formyl-3,5-dimethoxyphenoxy)-, ethyl ester | HCID 11001390 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a suspension of 4-formyl-3,5-dimethoxyphenol (22.6 g, 124 mmol) and potassium tert-butoxide (15.3 g, 136 mmol) in dimethylformamide (125 mL) was added ethyl 5-bromovalerate (28.5 g, 136 mmol) in dimethylformamide (125 mL) over a period of 20 min. The mixture was heated at 11 0° C. for 6 h and concentrated in vacuo. To the obtained product was added ethyl acetate (400 mL) and the mixture was filtered. The filtrate was washed with water (100 mL), 1 N sodium hydroxide (2×50 mL), and brine (3×100 mL), dried (magnesium sulfate), and concentrated in vacuo to 37 g of ethyl 5-(4-formyl-3,5-dimethoxyphenoxy)valerate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06939880B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-1cf60c876fbe4063b249ffb1131a01c0 |
| Source note | uspto-grants-2005_09 |