HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Acetyl-2-methyl-5-phenylthiophene → HCID 57594999, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Acetyl-2-methyl-5-phenylthiophene | HCID 2728765 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57594999 | HCID 57594999 | — |
Reaction Steps
To a solution of 1-(2-Methyl-5-phenyl-thiophen-3-yl)-ethanone (1.08 g, 5.00 mmole) in THF (20 mL), is added to LiBH4 (0.327 g, 15.0 mmole) in one portion at 0° C. The reaction is kept at 0° C. for 30 minutes and warmed up to room temperature for 2 hours. The reaction is quenched using NH4Cl(aq) (50 mL) at 0° C. The THF is removed on rota vapor, the aqueous solution is then extracted with ethyl acetate (3×50 mL). The combined organic solution is dried over Na2SO4 and concentrated to provide the titled compound as white solid, which is used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504433B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-dfee3024901a41058eca4305c84c80f0 |
| Source note | uspto-grants-2009_03 |