Succinic anhydride → N-n-hexyl 5-(3-carboxy-propionyloxy)-2-hydroxybenzamide

HRID 1746246Notes

Reaction equation

HRID 1746246 reaction equation
[CH2:1]([NH:7][C:8](=[O:17])[C:9]1[CH:14]=[C:13]([OH:15])[CH:12]=[CH:11][C:10]=1[OH:16])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[C:18]1(=[O:24])[O:23][C:21](=[O:22])[CH2:20][CH2:19]1>C(Cl)Cl>[CH2:1]([NH:7][C:8](=[O:17])[C:9]1[CH:14]=[C:13]([O:15][C:18](=[O:24])[CH2:19][CH2:20][C:21]([OH:23])=[O:22])[CH:12]=[CH:11][C:10]=1[OH:16])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]

Participants

4

Procedure

N-n-Hexyl 2,5-dihydroxybenzamide (1 g) is dissolved in 15 mL of methylene chloride. To the solution 0.75 g of succinic anhydride and 0.95 g of 4-N,N-dimethylaminopyridene is added. The reaction mixture is allowed to stir at ambient conditions over 24 hours. Solvent is removed and the residue is reconstituted in ethyl acetate and extracted twice with 1 N HCl to remove the catalyst. The organic layer is further extracted with saturated sodium chloride solution and dried over anhydrous sodium sulfate. Solvent is removed under reduced pressure to yield the product as an off-white powder.

Workup

  1. customSolvent is removed
  2. extractionextracted twice with 1 N HCl
  3. customto remove the catalyst
  4. extractionThe organic layer is further extracted with saturated sodium chloride solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. customSolvent is removed under reduced pressure

Sources & evidence

ORD record
ord-4e1693d4c0d54fa49751e5112261a731
Source dataset
uspto-grants-2015_10
Patent number
US09149530B2

Reaction notes

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