HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → Propargyl 6-phenylhexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-Phenylhexanoic Acid | HCID 79695 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Propargyl 6-phenylhexanoate | HCID 15790142 | — |
Reaction Steps
Two milliliters of a dry N,N-dimethylformamide solution of 618 mg of propargyl bromide is added by drops to a mixture of 1 g of 6-phenylhexanoic acid, 862 mg of potassium carbonate and 20 ml of dry N,N-dimethylformamide at room temperature with stirring. After stirring for 24 hours, the resultant solution is poured into an aqueous saturated ammonium chloride solution cooled with ice. The resulting mixture is then extracted twice with diethyl ether. The extracts are combined, washed with water and then with an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue is subjected to chromatography on silica gel to obtain propargyl 6-phenylhexanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405989 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-bbde34a4bb5842ad81577eb5bae35929 |
| Source note | uspto-grants-1995_04 |