Hydrochloric Acid → Benzoic acid, 4-(3-chloropropoxy)-3-methoxy-

HRID 384802Notes

Reaction equation

HRID 384802 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:15]=[CH:14][C:9]([C:10]([O:12]C)=[O:11])=[CH:8][C:7]=1[O:16][CH3:17].[OH-].[Na+].Cl>CO>[Cl:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:15]=[CH:14][C:9]([C:10]([OH:12])=[O:11])=[CH:8][C:7]=1[O:16][CH3:17]

Participants

5

Conditions

Temperature
40 °C

Procedure

In a 300 mL volume glass flask equipped with a stirrer, a thermometer and a dropping funnel were placed 18.2 g (69.7 mmol) of methyl 4-(3-chloropropoxy)-3-methoxybenzoate (purity: 98 wt. %) prepared by procedures similar to the procedures of Reference Example III-3, 69.7 mL of an aqueous sodium hydroxide (2 mol/L), and 69.7 mL of methanol. The resulting mixture was heated to 40° C. for 4 hours in an argon gas atmosphere. After the reaction was complete, the reaction mixture was cooled to 10° C. and neutralized by 69.7 mL of hydrochloric acid (2 mol/L), to precipitate a crystalline product. The crystalline product was collected by filtration and dried under reduced pressure. There was obtained 16.2 g (isolated yield: 93.8%, purity: 99% in terms of area percentage determined by high performance liquid chromatography) of 4-(3-chloropropoxy)-3-methoxybenzoic acid as a white crystalline product.

Workup

  1. customIn a 300 mL volume glass flask equipped with a stirrer
  2. temperaturethe reaction mixture was cooled to 10° C.
  3. customto precipitate a crystalline product
  4. filtrationThe crystalline product was collected by filtration
  5. customdried under reduced pressure

Sources & evidence

ORD record
ord-279f81db16fe416384e03e87d665f7f7
Source dataset
uspto-grants-2013_02
Patent number
US08367824B2

Reaction notes

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