HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Ethyl 4-(3-pentyloxyphenoxy)butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | 3-(Pentyloxy)phenol | HCID 15692229 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-(3-pentyloxyphenoxy)butyrate | HCID 22407863 | — |
Reaction Steps
A mixture of 7.3 g of 60% NaH in 190 ml of anhydrous dimethylformamide is cooled in an ice bath. To this mixture is added 22.0 g of 3-pentyloxyphenol dissolved in 50 ml of anhydrous dimethylformamide. This mixture is then stirred at room temperature for 45 minutes; 23.2 ml of ethyl 4-bromobutyrate are added; and the resultant mixture is stirred at 60° C. for 17 hours. The solvent is removed under vacuum and the residue worked up as above. The residue is flash chromatographed on normal phase silica gel using a gradient from hexane to a 4:1 ratio of hexane:ether to yield ethyl 4-(3-pentyloxyphenoxy)butyrate as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516767 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-22676dae95144dcb8920a1d205ec03c3 |
| Source note | uspto-grants-1996_05 |