Hydrochloric Acid → HCID 73554943, compound

HRID 591216Notes

Reaction equation

HRID 591216 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]([C:14]([O:16]C)=[O:15])[C:10]([O:12]C)=[O:11])[CH:5]=[C:6]([Cl:8])[CH:7]=1.[OH-].[Na+].Cl.ClCCl>CO.O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]([C:10]([OH:12])=[O:11])[C:14]([OH:16])=[O:15])[CH:5]=[C:6]([Cl:8])[CH:7]=1

Participants

7

Procedure

The crude 1,3-dimethyl 2-(3,5-dichlorophenyl)propanedioate form Step A was taken up in methanol (150 mL) and water (300 mL). To this mixture was added 50% aqueous sodium hydroxide (120 g, 1.5 mol) over 30 min at room temperature. The reaction mixture was stirred at room temperature for 18 hours and then cooled to 10° C. in an ice bath. The mixture was acidified with concentrated hydrochloric acid (135 mL of 37%) over 30 min while maintaining the temperature of the reaction mixture at less than 17° C. The reaction mixture was extracted with ethyl acetate (600 mL) and the organic phase was concentrated under vacuum to give a viscous oil. The crude oil was treated with dichloromethane (200 mL) and stirred till a thick slurry formed. The slurry was filtered and dried via suction filtration under a nitrogen blanket for 48 hours at room temperature to give a solid (76.0 g, 84% over 2 steps).

Workup

  1. temperaturecooled to 10° C. in an ice bath
  2. temperaturewhile maintaining the temperature of the reaction mixture at less than 17° C
  3. extractionThe reaction mixture was extracted with ethyl acetate (600 mL)
  4. concentrationthe organic phase was concentrated under vacuum
  5. customto give a viscous oil
  6. stirringstirred till a thick slurry
  7. customformed
  8. filtrationThe slurry was filtered
  9. customdried via suction filtration under a nitrogen blanket for 48 hours at room temperature
  10. customto give a solid (76.0 g, 84% over 2 steps)

Sources & evidence

ORD record
ord-1294050c030848afaad49fbc2584b7e0
Source dataset
uspto-grants-2016_01
Patent number
US09238650B2

Reaction notes

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