Hydrochloric Acid → HCID 86687872, compound

HRID 1910476Notes

Reaction equation

HRID 1910476 reaction equation
[CH3:1][C:2]1[O:6][C:5]([CH2:7][C:8]2[CH:9]=[C:10]([CH2:14][C:15]([O:17]C(C)(C)C)=[O:16])[CH:11]=[CH:12][CH:13]=2)=[N:4][N:3]=1.Cl>O1CCOCC1>[CH3:1][C:2]1[O:6][C:5]([CH2:7][C:8]2[CH:9]=[C:10]([CH2:14][C:15]([OH:17])=[O:16])[CH:11]=[CH:12][CH:13]=2)=[N:4][N:3]=1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 86687871HCID 86687871, compound

Product 1

HCID 86687872HCID 86687872, compoundYield 22.5%

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent2×

Procedure

To a mixture of tert-butyl 2-(3-((5-methyl-1,3,4-oxadiazol-2-yl)methyl)phenyl)acetate 1106 (0.127 g, 0.44 mmol) in dioxane (3 mL) was added 4N HCl in dioxane (1 mL) and stirred under an atmosphere of Argon for 2 hours. The volatiles were removed under reduced pressure and the residue diluted with water (5 mL) and the pH adjusted to 12 with 2.5 N NaOH. The mixture was washed with dichloromethane (4×2 mL) and the pH adjusted to 6 with 1 N HCl. The mixture was extracted with EtOAc (3×2 mL) and the organic layers combined, washed with brine and dried over Na2SO4. The Na2SO4 was removed by filtration and the volatiles removed under reduced pressure to give 0.023 g of 2-(3-((5-methyl-1,3,4-oxadiazol-2-yl)methyl)phenyl)acetic acid 1107.

Workup

  1. customThe volatiles were removed under reduced pressure
  2. additionthe residue diluted with water (5 mL)
  3. washThe mixture was washed with dichloromethane (4×2 mL)
  4. extractionThe mixture was extracted with EtOAc (3×2 mL)
  5. washwashed with brine
  6. dry with materialdried over Na2SO4
  7. customThe Na2SO4 was removed by filtration
  8. customthe volatiles removed under reduced pressure

Sources & evidence

ORD record
ord-b86a5209b82648c082e6a6d0dd000836
Source dataset
uspto-grants-2013_12
Patent number
US08604016B2

Reaction notes

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