1,1-Dichloroethane → HCID 59570398, compound

HRID 1880747Notes

Reaction equation

HRID 1880747 reaction equation
Cl[CH:2]([Cl:4])C.[Cl:5][C:6]1[CH:7]=[C:8]([CH:12]=[C:13]([Cl:15])[CH:14]=1)[C:9](Cl)=[O:10].[O:16]1CCCOO1>[Cl-].[Cl-].[Cl-].[Cl-].[Zr+4].O>[Cl:5][C:6]1[CH:7]=[C:8]([CH:12]=[C:13]([Cl:15])[CH:14]=1)[C:9]([O:16][CH2:2][Cl:4])=[O:10]

Participants

6

Procedure

To 10 ml of dichloroethane were added 1 g of zirconium tetrachloride and 1 g of 3,5-dichlorobenzoyl chloride, and the mixture was stirred at room temperature for 15 minutes. The mixture was cooled to 0° C., 0.16 g of trioxane was added, and the mixture was stirred for 1 hour, and further stirred at room temperature for 2 hours. 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. The residue was subjected to silica gel chromatography to obtain 1 g of chloromethyl 3,5-dichlorobenzoate.

Workup

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

Sources & evidence

ORD record
ord-6b60f0c8bd1c46148e9cf3faf82e4785
Source dataset
uspto-grants-2012_11
Patent number
US08318776B2

Reaction notes

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