Sodium Hydroxide → HCID 19004375, compound

HRID 2225779Notes

Reaction equation

HRID 2225779 reaction equation
C[O:2][C:3](=[O:28])[C:4](=[O:27])[C:5]1[C:10]([Cl:11])=[CH:9][C:8]([O:12][CH2:13][CH2:14][O:15][C:16]2[CH:25]=[CH:24][C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH:17]=2)=[CH:7][C:6]=1[Cl:26].[OH-].[Na+]>CO.O1CCCC1.O>[Cl:11][C:10]1[CH:9]=[C:8]([O:12][CH2:13][CH2:14][O:15][C:16]2[CH:25]=[CH:24][C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH:17]=2)[CH:7]=[C:6]([Cl:26])[C:5]=1[C:4](=[O:27])[C:3]([OH:28])=[O:2]

Participants

6

Procedure

A solution of 2,6-dichloro-4-[2-(2-naphthalenyloxy)ethoxy]-alpha-oxobenzeneacetic acid methyl ester(0.6 g) in warm methanol (10 mL) and tetrahydrofuran (10 mL) was treated with 1N sodium hydroxide (2 mL) and after 10 minutes the mixture was diluted with water and concentrated to remove the organic solvents. The residue was acidified with excess hydrochloric acid and extracted with dichloromethane containing a little tetrahydrofuran. The organic layer was washed with water, dried (Na2SO4), filtered and evaporated to give crude product. Crystallization from acetone-hexane provided 0.53 g of purified 2,6-dichloro-4-[2-(2-naphthalenyloxy)ethoxy]-alpha-oxobenzeneacetic acid as a colorless solid, mp 155°-156° C.

Workup

  1. concentrationconcentrated
  2. customto remove the organic solvents
  3. extractionextracted with dichloromethane containing a little tetrahydrofuran
  4. washThe organic layer was washed with water
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated
  8. customto give crude product
  9. customCrystallization from acetone-hexane

Sources & evidence

ORD record
ord-3b9c4d4edc164d8ebb7f9bb45a0040c0
Source dataset
uspto-grants-1994_09
Patent number
US05344843

Reaction notes

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