Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Acetate | HCID 6584 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 12995921 | HCID 12995921 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67314184 | HCID 67314184 | 79% |
Reaction Steps
NaHMDS (428 mL, 1 M in hexane) was dissolved in THF (356 mL) and the resulting solution was cooled to −78° C. Methyl acetate (28.3 mL, 356 mmol) was added over 15 minutes and the reaction mixture was stirred at −78° C. for 1 h after which a solution (R,E)-N-(cyclopropylmethylene)-2-methylpropane-2-sulfinamide (26) (12.3 g, 71.3 mmol) in THF (50 mL) was added over 15 minutes. The reaction mixture was warmed to −20° C. and stirred at this temperature for 3 h after which HPLC indicated that the reaction was complete. The resulting solution was diluted with EtOAc (400 mL) and washed with sat. aq. NaHCO3 (200 mL). The organic phase was dried (Na2SO4), filtered, concentrated under vacuum and purified on a silica gel column (eluant hexane/EtOAc, 9/1 to 1/1 to give 16.3 g (79%) of (5S)-methyl 5-cyclopropyl-5-[(R)-1,1-dimethylethylsulfinamido]-3-oxopentanoate (27). Retention time (min)=1.397 method [1], MS (m/z) 290.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977368B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-ed44857a517c493b9f523009e1831295 |
|---|
| Source note | uspto-grants-2011_07 |
|---|