HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-(3-Hydroxy-1-butynyl)-2,2'-bithiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Butyn-2-ol | HCID 16239 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-Iodo-2,2'-bithiophene | HCID 11323778 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-(3-Hydroxy-1-butynyl)-2,2'-bithiophene | HCID 18920426 | 93% |
Reaction Steps
To the mixture of 1 g (14.3 mmole) of 3-hydroxy-1-butyne, 10 ml of benzene and 2.78 g of 5-iodo-2,2'-bithiophene (9.52 mmole) was added 0.15 g of CuI, 0.15 g of benzyltriethylammonium chloride, 0.2 g of Pd(PPh3)4 and then 15 ml of NaOH solution (2.5N) at room temperature and stirred for 2 hours. 4 ml of NH4Cl solution was then added. The reaction solution was extracted with ethyl acetate. The extract was washed with 10 ml of HCl (10%) for 3 times, 50 ml of water twice, and dried over anhydrous magnesium sulfate. The crude product was purified by silica gel column chromatography. From the eluate of ethyl acetate/n-hexane (3/1) 2.07 g of yellow solid product (93%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05747525 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-cb04652714c34ae8af08490bfb352262 |
| Source note | uspto-grants-1998_05 |