Hydrochloric Acid → HCID 86687872, compound
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]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- customThe volatiles were removed under reduced pressure
- additionthe residue diluted with water (5 mL)
- washThe mixture was washed with dichloromethane (4×2 mL)
- extractionThe mixture was extracted with EtOAc (3×2 mL)
- washwashed with brine
- dry with materialdried over Na2SO4
- customThe Na2SO4 was removed by filtration
- customthe volatiles removed under reduced pressure
Sources & evidence
- ORD record
- ord-f9d30f80ae7d44d989d7fa6c7e5bd154
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08865718B2
Reaction notes
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