1,1-Dichloroethane → HCID 10130258, compound

HRID 1880743Notes

Reaction equation

HRID 1880743 reaction equation
Cl[CH:2]([Cl:4])C.[CH3:5][C:6]1[CH:14]=[CH:13][C:9]([C:10](Cl)=[O:11])=[CH:8][CH:7]=1.[O:15]1CCCOO1>[Cl-].[Cl-].[Cl-].[Cl-].[Zr+4].O>[CH3:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([O:15][CH2:2][Cl:4])=[O:11])=[CH:8][CH:7]=1

Participants

6

Procedure

To 10 ml of dichloroethane were added 1.36 g of zirconium tetrachloride and 1 g of 4-methylbenzoyl chloride, and the mixture was stirred at room temperature for 20 minutes. The mixture was cooled to 0° C., 0.22 g of trioxane was added, and the mixture was stirred at room temperature for 1 hour. Water was added slowly at 0° C., the resultant solution was extracted with chloroform three times, and the organic layers were combined, washed with an aqueous saturated sodium bicarbonate solution and an aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated to obtain 0.7 g of chloromethyl 4-methylbenzoate.

Workup

  1. temperatureThe mixture was cooled to 0° C.
  2. stirringthe mixture was stirred at room temperature for 1 hour
  3. extractionthe resultant solution was extracted with chloroform three times
  4. washwashed with an aqueous saturated sodium bicarbonate solution
  5. dry with materialan aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-e64a9082541447af9d1ba3abd948188c
Source dataset
uspto-grants-2012_11
Patent number
US08318776B2

Reaction notes

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