HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(3-Phenyl-1,2,4-oxadiazol-5-yl)butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 3-(3-phenyl-1,2,4-oxadiazol-5-yl)butanoate | HCID 66725791 | — |
| Product | 4-(3-Phenyl-1,2,4-oxadiazol-5-yl)butanoic acid | HCID 667252 | 99% |
Reaction Steps
To a solution of methyl 3-(3-phenyl-1,2,4-oxadiazol-5-yl)butanoate (1.53 g, 6.21 mmole) in methanol (10 ml) was added 1N NaOH (10 mL). After stirring at room temperature for 2 hours, the reaction solution was acidified to pH=3-4 with 6N HCl under an ice bath and then extracted with ethyl acetate three times. The combined organic layers were washed with water and then brine, dried over Na2SO4, filtered and concentrated to give the desired product (1.44 g, 99% yield) as white solid. LCMS calculated for C12H13N2O3 (M+H): 233.1. Found: 233.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703783B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-a8117ef852d24070b3647937c659fcf4 |
| Source note | uspto-grants-2014_04 |