HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl acetate → tert-butyl (5S)-6-chloro-5-hydroxy-3-oxohexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | Ethyl (3S)-4-chloro-3-hydroxybutanoate | HCID 7019277 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | tert-butyl (5S)-6-chloro-5-hydroxy-3-oxohexanoate | HCID 7022053 | — |
Reaction Steps
Separately, 240 mg (6 mmol equivalent) of sodium hydride (60% in mineral oil) was washed with hexane and, then, 6 ml of tetrahydrofuran was added. Then, at 5° C., 1.71 g (18.0 mmol) of magnesium chloride, 1.74 g (15.0 mmol) of tert-butyl acetate and 1.0 g (6 mmol) of ethyl(3S)-4-chloro-3-hydroxybutyrate were added and the mixture was stirred for 30 minutes. To this mixture, the lithium diisopropylamide solution prepared above was added dropwise over 10 minutes at the same temperature and the reaction mixture was further stirred at an elevated temperature of 25° C. for 3 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472544B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-a5b5c6ba3bcc418cb3707e40ce80c592 |
| Source note | uspto-grants-2002_10 |