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Water → (R)-2-methyl-propane-2-sulfinic acid [(S)-1-(4-bromo-2-methyl-phenyl)-ethyl]amide

HRID 1640855
Notes
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Reaction equation

HRID 1640855 reaction equation
C([BH-](C(CC)C)C(CC)C)(CC)C.[Li+].[Br:15][C:16]1[CH:21]=[CH:20][C:19]([C:22](=[N:24][S@@:25]([C:27]([CH3:30])([CH3:29])[CH3:28])=[O:26])[CH3:23])=[C:18]([CH3:31])[CH:17]=1.O>O1CCCC1>[Br:15][C:16]1[CH:21]=[CH:20][C:19]([C@@H:22]([NH:24][S@@:25]([C:27]([CH3:30])([CH3:29])[CH3:28])=[O:26])[CH3:23])=[C:18]([CH3:31])[CH:17]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 3611392Lithium tri-s-butylborohydrideHCID 86649414(R)-2-Methyl-propane-2-sulfinic acid [1-(4-bromo-2-methyl-phenyl)-ethylidene]-amide

Product 1

HCID 58102376(R)-2-methyl-propane-2-sulfinic acid [(S)-1-(4-bromo-2-methyl-phenyl)-ethyl]amide

Reagents, catalysts & solvents 1

HCID 8028Tetrahydrofuran
Solvent

Procedure

Lithium tri-sec-butylborohydride (1 mol/L in tetrahydrofuran, 59.2 mL) was added to a solution of (R)-2-methyl-propane-2-sulfinic acid [1-(4-bromo-2-methyl-phenyl)-ethylidene]-amide (6.24 g) in tetrahydrofuran (50 mL) chilled in an ice bath. The solution was stirred for 2 h while warming to room temperature in the cooling bath. The solution was then cooled again in an ice bath prior to the careful addition of water. The resulting mixture was extracted with ethyl acetate and the combined extracts were washed with water, saturated aqueous NaHCO3 solution, and brine. After drying (MgSO4) and evaporating the solvent, the title compound was obtained that was directly submitted to the next reaction step. Yield: 8.85 g (ca. 75% pure); Mass spectrum (ESI−): m/z=318/320 (Br) [M+H]+.

Workup

  1. temperaturechilled in an ice bath
  2. temperatureThe solution was then cooled again in an ice bath
  3. extractionThe resulting mixture was extracted with ethyl acetate
  4. washthe combined extracts were washed with water, saturated aqueous NaHCO3 solution, and brine
  5. dry with materialAfter drying (MgSO4)
  6. customevaporating the solvent

Sources & evidence

ORD record
ord-6c781cc29605483386af1e47b643ecb6
Source dataset
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08114868B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes