Ammonia → 2-Iodo-5-propoxy-benzamide

HRID 76136Notes

Reaction equation

HRID 76136 reaction equation
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([O:10][CH2:11][CH2:12][CH3:13])[CH:7]=[CH:6][C:5]=1[I:14].[OH-].[Na+].Cl.C1N=C[N:21](C(N2C=NC=C2)=O)C=1.N>O.CO>[I:14][C:5]1[CH:6]=[CH:7][C:8]([O:10][CH2:11][CH2:12][CH3:13])=[CH:9][C:4]=1[C:3]([NH2:21])=[O:2]

Participants

8

Conditions

Temperature
50 °C

Procedure

A mixture of 4.12 g (12.9 mmol) methyl-5-propoxy-2-iodobenzoate and 60 mL MeOH is charged with 129 mL (258 mmol) 2N aq. NaOH solution. The resulting mixture is stirred at 50° C. for 3 h. Then the mixture was acidified to pH5 with 1 M aq. HCl and extracted with EtOAc (2×). The combined organic layers are washed with water and brine, dried with Na2SO4 and the solvent is removed in vacuo. The crude product from the previous saponification is added to 30 mL THF, charged with 2.04 g (12.6 mmol) CDI and stirred at r.t. for 1 h. More 0.5 eq CDI are added and stirring is continued for 20 min. To this mixture are added dropwise 20 mL of 35% ammonia in water and the resulting reaction mixture is stirred at r.t. for 5 min. The solvent is partly removed in vacuo until precipitation of a white solid occurs. The product is filtered and dried at 40° C. in vacuo.

Workup

  1. extractionextracted with EtOAc (2×)
  2. washThe combined organic layers are washed with water and brine
  3. dry with materialdried with Na2SO4
  4. customthe solvent is removed in vacuo
  5. additionThe crude product from the previous saponification is added to 30 mL THF
  6. stirringstirred at r.t. for 1 h
  7. stirringstirring
  8. waitis continued for 20 min
  9. customthe resulting reaction mixture
  10. stirringis stirred at r.t. for 5 min
  11. customThe solvent is partly removed in vacuo until precipitation of a white solid
  12. filtrationThe product is filtered
  13. customdried at 40° C. in vacuo

Sources & evidence

ORD record
ord-2f936e49686448d4aebb2ada87fdb712
Source dataset
uspto-grants-2014_09
Patent number
US08835472B2

Reaction notes

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