HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → N-(4-(2-ethylbutanoyl)phenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | N-(4-Butyrylphenyl)acetamide | HCID 4304236 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-(2-ethylbutanoyl)phenyl)acetamide | HCID 43160160 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of N-(4-butyrylphenyl)acetamide (3 g, 14.6 mmol) in THF (300 mL) was added 2.0 M LDA in THF (18.3 mL) at −78° C. and then the reaction mixture was stirred for 1 h at −78° C. Iodoethane was added and stirred overnight at RT. The reaction mixture was quenched with sat. aq. NH4Cl and then extracted with ethyl acetate. The combined organic layers were dried over MgSO4, filtered and then concentrated. The crude product was purified by preparative TLC using 50% ethyl acetate in hexane as eluent to afford N-(4-(2-ethylbutanoyl)phenyl)acetamide as white solid. MS (ES+): m/z 234.28 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513291B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-acc302f343d14b3a8b57885f9d9dcb49 |
| Source note | uspto-grants-2013_08 |