HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Fluorohex-5-ynoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Acetyl-2-fluoro-6-(trimethylsilyl)-5-hexynoic acid ethyl ester | HCID 13393080 | — |
| Reactant | Ethanol sodium ethoxide | HCID 23706232 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Fluorohex-5-ynoic acid | HCID 13044950 | 101% |
Reaction Steps
To a solution of 2-acetyl-2-fluoro-6-(trimethylsilyl)-5-hexynoic acid ethyl ester (6.63 g) in ethanol (20 ml) was added 27 ml of 2.65 M sodium ethoxide/ethanol. After 18 hours, 7 ml of 4 N sodium hydroxide was added. After 6 hours, the solvent was removed by rotary evaporation and the residual materials partitioned between ethyl ether and dilute hydrochloric acid. The organic layer was dried (MgSO4) and the solvent removed by rotary evaporation to give an oil which was vacuum distilled to yield 3.2 g of 2-fluoro-5-hexynoic acid; b.p. 118°/14 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04345084 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-69845f60fba54ff58ea099e1cdaf8035 |
| Source note | uspto-grants-1982_08 |