HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → (4-Fluoro-benzylamino)-phenyl-acetic acid hydrochloride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-Phenylglycine | HCID 3866 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | (4-Fluoro-benzylamino)-phenyl-acetic acid hydrochloride | HCID 67425426 | — |
Reaktionsschritte
4-Fluorobenzaldehyde (0.25 mL, 2.38 mmol), 2-amino-2-phenylacetic acid (300 mg, 1.98 mmol) and NaOH (79 mg, 1.98 mmol) are dissolved in MeOH (20 mL) and stirred at RT overnight. The reaction is cooled at 0° C. and NaBH4 (150 mg, 3.97 mmol) is added. After being stirred at 0° C. for 30 minutes, the reaction is judged complete by UPLC-MS analysis. 4M HCl in dioxane is added dropwise till pH 5 and the precipitate is collected by suction filtration, washed with Et2O and dried under vacuum at 40° C. to obtain intermediate I129 as a white solid (587 mg, quantitative yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08835682B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-f545af928ca34d60ae9e8a8e446c8507 |
| Quellennotiz | uspto-grants-2014_09 |