Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Acetate | HCID 6584 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | HCID 86649302 | HCID 86649302 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68731966 | HCID 68731966 | 46% |
Reaction Steps
A solution of i-Pr2NH in THF (25 mL) was cooled to −78° C., n-BuLi (2.5M, 2 mL) was added and the solution was stirred for 1 h. Then methyl acetate (4.48 mmol, 278 mg) was added and the mixture was stirred for 30 min. To this solution Ti(Oi-Pr)3Cl (1 M, 9.4 mL) was added. After 0.5 h, (S)-2-methyl-N-(1-phenylethylidene)propane-2-sulfinamide (500 mg, 2.24 mmol) dissolved in THF (1 mL) was added. The mixture was stirred at −78° C. for 3 h. The reaction was quenched with NH4Cl and warmed to rt. The mixture was diluted with water and filtered. The solid was washed with H2O/EtOAc and filtered. The combined organic layers were washed with brine, dried over Na2SO4, and concentrated. The residue was purified by preparative TLC to afford (R)-methyl 3-((S)-1,1-dimethylethylsulfinamido)-3-phenylbutanoate (305 mg, 46%). 1H NMR (CDCl3): 1.24 (s, 9H), 1.68 (s, 3H), 3.08 (s, 2H), 3.53 (s, 3H), 5.46 (s, 1H), 7.15-7.18 (m, 1H), 7.23-7.30 (m, 2H), 7.30-7.36 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079861B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-1097d4c56598437eba6e96256339d1c9 |
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| Source note | uspto-grants-2015_07 |
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