1,4-Dibromobutane → 1-Bromo-4-(tert-butylsulfanyl)butane

HRID 1363009Notes

Reaction equation

HRID 1363009 reaction equation
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5]Br.[CH3:7][C:8]([S-:11])([CH3:10])[CH3:9].[Na+]>CN(C=O)C>[CH3:7][C:8]([S:11][CH2:5][CH2:4][CH2:3][CH2:2][Br:1])([CH3:10])[CH3:9]

Participants

4

Conditions

Temperature
70 °C

Procedure

A solution of 1,4-dibromobutane (commercially available, for example, from Aldrich) (4.7 ml, 40 mmol) in DMF (10 ml) was treated with sodium 2-methyl-2-propanethiolate (commercially available, for example, from Aldrich) (3.36 g, 30 mmol) and the mixture was heated for 23 h at 70° C. The mixture was allowed to cool to room temperature, and partitioned between water and EtOAc. The organic solution was washed with water (×4), aqueous sodium bicarbonate solution, brine, dried (MgSO4), and evaporated. The residue was purified by flash column chromatography on silica (200 g) eluting with 0-50% EtOAc-cyclohexane to give the title compound (1.4 g, 21%): 1H NMR δ (CDCl3) 3.46 (2H, t, J=7 Hz), 2.96 (2H, t, J=7 Hz), 2.15-2.03 (4H, m), 1.44 (9H, s).

Workup

  1. temperatureto cool to room temperature
  2. custompartitioned between water and EtOAc
  3. washThe organic solution was washed with water (×4), aqueous sodium bicarbonate solution, brine
  4. dry with materialdried (MgSO4)
  5. customevaporated
  6. customThe residue was purified by flash column chromatography on silica (200 g)
  7. washeluting with 0-50% EtOAc-cyclohexane

Sources & evidence

ORD record
ord-6c402eac676c4b199246a3dd0ac75a9d
Source dataset
uspto-grants-2011_02
Patent number
US07884114B2

Reaction notes

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