HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-Fluoro-5-phenoxybenzyl 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 2-Fluoro-5-phenoxybenzyl bromide | HCID 14579132 | — |
| Reactant | 3-(4-Chlorophenoxy)-2,2-dimethylcyclopropanecarboxylic acid | HCID 20304961 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluoro-5-phenoxybenzyl 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylate | HCID 54440629 | — |
Reaction Steps
To a mixture of 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylic acid (2.77 mmol), potassium carbonate (3.25 mmol) and hexamethylphosphoric triamide (HMPT) (3 ml), with stirring and under nitrogen, at RT, is added 2-fluoro-5-phenoxybenzyl bromide (2.77 mmol) in THF. The reaction is stirred at RT for about 48 hours and then worked up by partition between water/ether. The organic phase is washed with water and brine, dried over potassium carbonate, filtered and the solvent is removed from the filtrate. The residue is plated on prep. TLC plates developing with 10% ether/hexane to yield 2-fluoro-5-phenoxybenzyl 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225533 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-bd1c0c1c5b2d448aa9897a4eb2fd9cf3 |
| Source note | uspto-grants-1980_09 |