HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium diisopropylamide → 4-Trimethylsilyloxy-5-(1-hydroxy-6-methoxycarbonylhexyl)-4-octyl-2-cyclopentenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Methyl 7-oxoheptanoate | HCID 3015770 | — |
| Reactant | (4R)-4-trimethylsilyloxy-4-octyl-2-cyclopentenone | HCID 13767761 | — |
| Reactant | Isopropylamide | HCID 18378000 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Trimethylsilyloxy-5-(1-hydroxy-6-methoxycarbonylhexyl)-4-octyl-2-cyclopentenone | HCID 13767764 | — |
Reaction Steps
Under a nitrogen atmosphere at -78° C., a solution of 200 mg (0.71 mmole) of (4R)-4-trimethylsilyloxy-4-octyl-2-cyclopentenone in 2 ml of tetrahydrofuran was added to a solution of LDA prepared from 93 mg (0.92 mmole) of isopropylamide and 590 microliters of n-butyllithium (as a 10 W/V % hexane solution) in 3 ml of tetrahydrofuran, and the mixture was stirred for 1 hour. Then, a solution of 146 mg (0.92 mmole) of methyl 6-formylhexanoate in 2 ml of tetrahydrofuran was added, and the mixture was stirred at -78° C. for 2 hours. The reaction was terminated by adding an aqueous solution of ammonium chloride. The reaction mixture was extracted with ether, and the extract was dried over anhydrous magnesium sulfate, filtered and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04711895 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-5289f19d942d4f9d850c5379261cf8ac |
| Source note | uspto-grants-1987_12 |