Reaction #595318

ord-5f5bff0798034470b3f506fc65b38bb7

Reaction equation

CC(C)[C@@H](Br)C(=O)O
(R)-(+)-2-bromo-3-methylbutyric acid
[Cs+].[O-]C(=S)c1ccccc1
cesium thiobenzoate
CC(C)[C@H](SC(=O)c1ccccc1)C(=O)O
(S)-2-benzoylthio-3-methylbutanoic acid
Yield 72.6%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Washwashed with H2O (4×40 mL)
  2. 2
    DryingThe ethereal layer was dried (Na2SO4)
  3. 3
    Concentrationconcentrated
  4. 4
    OtherThe crude residue was recrystallized from hexanes

Procedure

To a solution of (R)-(+)-2-bromo-3-methylbutyric acid (4.20 g, 23.2 mmol) in DMF (41 mL) was added cesium thiobenzoate (6.08 g, 22.5 mmol). The mixture was stirred at rt for 20 h. The resulting solution was diluted with ether (200 mL) and washed with H2O (4×40 mL). The ethereal layer was dried (Na2SO4), and concentrated. The crude residue was recrystallized from hexanes to afford (S)-2-benzoylthio-3-methylbutanoic acid as a pale yellow solid (3.89 g, 72%); 1H NMR (300 MHz, CDCl3) δ 1.09 (d, J=7.4 Hz, 3H), 1.11 (d, J=7.4 Hz, 3H), 2.40 (m, 1H), 4.37 (d, J=5.9 Hz, 1H), 7.45 (t, J=7.4 Hz, 2H), 7.57 (t, J=7.4 Hz, 1H), 7.97 (d, J=7.4 Hz, 2H), 12.0 (br s, 1H); 13C NMR (75 MHz, CDCl3) δ 19.8, 20.6, 30.5, 53.1, 127.6, 128.8, 133.9, 136.3, 177.9, 190.3; IR (neat) 3100, 2967, 1709, 1669 cm−1; [α]D22=−94.2 (c 1, CH2Cl2).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09095565B2uspto-grants-2015_08