HuagongsheHuagongshe Chemistry Print Report · For research reference only
epsilon-CAPROLACTONE → 6-(4-Fluoro-3-methylbenzyloxy)hexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | epsilon-CAPROLACTONE | HCID 10401 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(Bromomethyl)-1-fluoro-2-methylbenzene | HCID 2778135 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-(4-Fluoro-3-methylbenzyloxy)hexanoic acid | HCID 59512578 | 94% |
Reaction Steps
To a solution of oxepan-2-one (0.562 g, 4.925 mmol) and 4-fluoro-3-methylbenzyl bromide (3.000 g, 14.774 mmol) in 20 mL of toluene, was added KOH (1.382 g, 24.625 mmol). The mixture was refluxed for 86 h. After cooling to room temperature, the reaction mixture was diluted with water (80 mL) and washed with ether. The aqueous layer was acidified with concentrated HCl to pH=2 and extracted with ether (50 mL×3). The combined organic extracts dried (Na2SO4), filtered, and concentrated under reduced pressure to give the title compound as colorless oil which was used directly in the next step without further purification (1.173 g, 94% yield). LC-MS: tR=8.0 min, m/z 277 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242174B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-ac8070f6620045d08ced0ce0e8c70969 |
| Source note | uspto-grants-2012_08 |