Dimethyl Sulfoxide → Benzenepentanal

HRID 1107102Notes

Reaction equation

HRID 1107102 reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[C:11]1([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][OH:22])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(N(CC)CC)C>C(Cl)Cl>[C:11]1([CH2:17][CH2:18][CH2:19][CH2:20][CH:21]=[O:22])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

6

Conditions

Temperature
-55 °C

Procedure

To a mechanically stirred solution of oxalyl chloride (21.6 g; 170 mmol) in dry CH2Cl2 (400 mL) at -78° C. is added DMSO (22.3 g; 360 mmol) dropwise over 45 minutes. After stirring 15 minutes 5-phenylpentanol (25 g; 150 mmol) is added and the internal temperature is allowed to warm to -55° C. After stirring at this temperature for 30 minutes the reaction is cooled to -78° C. and triethylamine (104 mL; 750 mmol) is added slowly over 20 minutes. After stirring 15 minutes the reaction bath is removed and the temperature is allowed to warm to 20° C. over 40 minutes. The reaction mixture is then washed with 500 mL water. The water layer is then back-extracted with CH2Cl2 (2×50 mL). The combined organic fractions are washed with 300 mL 2 N HCl, 100 mL water, 200 mL NaHCO3, 100 mL brine and dried (MgSO4). The solution is concentrated in vacuo to obtain 5-phenylpentanal (25 g) which is used directly in Step B.

Workup

  1. additionis added
  2. temperatureis cooled to -78° C.
  3. stirringAfter stirring 15 minutes the reaction bath
  4. customis removed
  5. temperatureto warm to 20° C. over 40 minutes
  6. washThe reaction mixture is then washed with 500 mL water
  7. extractionThe water layer is then back-extracted with CH2Cl2 (2×50 mL)
  8. washThe combined organic fractions are washed with 300 mL 2 N HCl, 100 mL water, 200 mL NaHCO3, 100 mL brine
  9. dry with materialdried (MgSO4)
  10. concentrationThe solution is concentrated in vacuo

Sources & evidence

ORD record
ord-3c6f885bc8774f6c86eaaef5aad50c8c
Source dataset
uspto-grants-2000_05
Patent number
US06057369

Reaction notes

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