HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 54371494, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Bromo-4-fluorophenol | HCID 605472 | — |
| Reactant | HCID 54106401 | HCID 54106401 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54371494 | HCID 54371494 | 70% |
Reaction Steps
To MeOH (140 mL) solution containing KOH (4.73 g, 84.3 mmol) at 22° C. was added 2-bromo-4-fluorophenol (16.09 g, 84.2 mmol) and 2-pentyne-1,5-diol ditosylate (11.47 g, 28.1 mmol). After stirring 20 h acetic acid (3.5 mL) was added and the reaction stirred 1 h. The reaction was concentrated in vacuo and the residue extracted with CH2Cl2 (75 mL) and saturated K2CO3 (75 mL). The organic phase was separated and washed with saturated K2CO3. The aqueous phase was washed with CH2Cl2 (2×30 mL). The combined CH2 Cl2 layers were dried with dried with MgSO4, filtered, concentrated in vacuo. Silica gel chromatography (9:1 Hexane:EtOAc) yielded the title compound as a viscous oil (8.39 g, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763444 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-0b248aaf49e84f72bc559fa7c96883e1 |
| Source note | uspto-grants-1998_06 |