HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-[3-(3-Bromophenyl)oxetan-3-yl]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-[3-(3-bromophenyl)oxetan-3-yl]acetate | HCID 57969689 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[3-(3-Bromophenyl)oxetan-3-yl]acetic acid | HCID 57969737 | 105.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Ethyl 2-[3-(3-bromophenyl)oxetan-3-yl]acetate (1.5 g, 4.513 mmol) was dissolved in MeOH (25 mL) and cooled to 0° C. NaOH (9.026 mL of 1M, 9.026 mmol) was added and the reaction allowed to warm to rt overnight. The solvent was removed under reduced pressure and the solution neutralised with 2 eq of HCl (1M soln, 9.026 mL) and extracted with ethyl acetate. The combined organics were washed with brine, dried over MgSO4, filtered and the solvent removed under reduced pressure to give 2-[3-(3-bromophenyl)oxetan-3-yl]acetic acid as a viscous yellow oil (1.287 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367697B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-ff646fd7ec88497889b50a53a5775241 |
| Source note | uspto-grants-2013_02 |