p-Chlorothiophenol → HCID 11507705, compound

HRID 2245780Notes

Reaction equation

HRID 2245780 reaction equation
[CH2:1]([O:3][C:4](=[O:12])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10]Br)[CH3:2].C(N(CC)CC)C.[Cl:20][C:21]1[CH:26]=[CH:25][C:24]([SH:27])=[CH:23][CH:22]=1>ClCCl>[CH2:1]([O:3][C:4](=[O:12])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][S:27][C:24]1[CH:25]=[CH:26][C:21]([Cl:20])=[CH:22][CH:23]=1)[CH3:2]

Participants

5

Procedure

To a solution of 7-bromoheptanoic acid ethyl ester (2.5 mL, 12.8 mmol) and triethylamine (2 mL, 14.3 mmol) in dichloromethane (10 mL) was added 4-chlorothiophenol (1.86 g, 12.8 mmol) under an atmosphere of argon. The mixture was stirred at reflux for 2 hours after which it was concentrated under reduced pressure. The oil was dissolved in ethyl acetate (50 mL) and then washed successively with saturated aqueous sodium hydrogen carbonate (25 mL), distilled water (25 mL) and brine (25 mL). The organic layer was then dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to give an yellow oil that was purified by flash chromatography (1:9 diethyl ether:40-60° C. petroleum ether). The title compound was obtained as a colourless oil (3.3 g, 87%).

Workup

  1. temperatureat reflux for 2 hours after which it
  2. concentrationwas concentrated under reduced pressure
  3. dissolutionThe oil was dissolved in ethyl acetate (50 mL)
  4. washwashed successively with saturated aqueous sodium hydrogen carbonate (25 mL)
  5. distillationdistilled water (25 mL) and brine (25 mL)
  6. dry with materialThe organic layer was then dried over anhydrous MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customto give an yellow oil that
  10. customwas purified by flash chromatography (1:9 diethyl ether:40-60° C. petroleum ether)

Sources & evidence

ORD record
ord-73a6338d035241ee8cdf60b1fc02ba16
Source dataset
uspto-grants-2010_03
Patent number
US07683185B2

Reaction notes

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