Hydrochloric Acid → HCID 75041477, compound

HRID 551632Notes

Reaction equation

HRID 551632 reaction equation
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH:11]([CH:14]([CH2:17][CH:18]=[CH2:19])[CH2:15][OH:16])([CH3:13])[CH3:12].C(N(CC)CC)C.Cl>ClCCl>[CH:11]([CH:14]([CH2:17][CH:18]=[CH2:19])[CH:15]=[O:16])([CH3:13])[CH3:12]

Participants

7

Conditions

Temperature
-78 °C

Procedure

Dimethyl sulfoxide (18.70 mL, 263.3 mmol) was added dropwise over 15 minutes to a dichloromethane (290 mL) solution of oxalic acid chloride (17.30 g, 136.3 mmol) cooled to −78° C., and the mixture was then stirred at −78° C. for 15 minutes. Subsequently, a dichloromethane (75 mL) solution of 2-isopropylpent-4-en-1-ol (11.30 g, 88.1 mmol) was added dropwise thereto over 30 minutes, and the mixture was stirred at −78° C. for 1 hour. Triethylamine (62.40 g, 616.7 mmol) was added dropwise thereto over 5 minutes, and the mixture was then stirred at room temperature for 2 hours. The mixture was neutralized with 2 N hydrochloric acid (320 mL). The organic layer was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to obtain a yellow oil substance as a mixture containing the compound of interest. This compound was used in the next reaction without being further purified.

Workup

  1. waitover 30 minutes
  2. stirringthe mixture was stirred at −78° C. for 1 hour
  3. waitover 5 minutes
  4. stirringthe mixture was then stirred at room temperature for 2 hours
  5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  6. distillationThen, the solvent was distilled off under reduced pressure
  7. customto obtain a yellow oil substance as a mixture
  8. additioncontaining the compound of interest
  9. customThis compound was used in the next reaction

Sources & evidence

ORD record
ord-98412459f6234328ba83284379042b4f
Source dataset
uspto-grants-2011_05
Patent number
US07947738B2

Reaction notes

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