Pyridine → 1-Chloro-5-ethoxyheptane

HRID 569222Notes

Reaction equation

HRID 569222 reaction equation
[CH2:1]([O:3][CH:4]([CH2:10][CH3:11])[CH2:5][CH2:6][CH2:7][CH2:8]O)[CH3:2].N1C=CC=CC=1.S(Cl)([Cl:20])=O>O>[Cl:20][CH2:8][CH2:7][CH2:6][CH2:5][CH:4]([O:3][CH2:1][CH3:2])[CH2:10][CH3:11]

Participants

5

Procedure

5-Ethoxyheptanol (238 g, 1.49 moles) is diluted in pyridine (128 g, 1.62 moles). The solution is stirred at room temperature and thionyl chloride (388 g, 3.22 moles) is added dropwise over 2 hours, after which time the reaction is heated in a 70° C. water bath for 2 additional hours. Water (700 ml) is added to the reaction and the organic layer separated. The aqueous layer is extracted with hexane (3×400 ml) and the extracts combined with the organic phase. The organic phase is then washed with a 10% sodium hydroxide solution (1000 ml). The solvent volume is reduced under vacuum and the residue dried over anhydrous magnesium sulfate. The remaining solvent is removed leaving 1-chloro-5-ethoxyheptane as a clear light yellow oil. The crude product is fractionally distilled under reduced pressure leaving 1-chloro-5-ethoxyheptane as a clear, colorless oil (162 g, 1.13 moles), BP 96° C./9.5 cm Hg.

Workup

  1. temperatureafter which time the reaction is heated in a 70° C. water bath for 2 additional hours
  2. customthe organic layer separated
  3. extractionThe aqueous layer is extracted with hexane (3×400 ml)
  4. washThe organic phase is then washed with a 10% sodium hydroxide solution (1000 ml)
  5. dry with materialthe residue dried over anhydrous magnesium sulfate
  6. customThe remaining solvent is removed

Sources & evidence

ORD record
ord-d53bccdd59594cf68dd50e1d09fe08b4
Source dataset
uspto-grants-1988_03
Patent number
US04731458

Reaction notes

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