HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64450Erstellt: 25. Oktober 2026
Ammonium Chloride → methyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoate
https://huagongshe.com/reaction/64450
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | methyl 3-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]benzoate | HCID 90072367 | — |
| Edukt | HCID 178443585 | HCID 178443585 | — |
| Edukt | HCID 178467792 | HCID 178467792 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | methyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoate | HCID 86713465 | — |
Reaktionsschritte
To a solution of 500 mg of methyl 3-[(E)-{[(S)-tert-butylsulfinyl]imino}methyl]benzoate in 12 ml of THF was added 0.50 ml of a 1 M diethylzinc/hexane solution at −78° C., followed by stirring at the same temperature for 5 minutes. 0.80 ml of a 3 M ethylmagnesium bromide/diethyl ether solution was added thereto at −78° C., followed by stirring at the same temperature for 2 hours. To the reaction mixture were added a saturated aqueous ammonium chloride solution and ethyl acetate to carry out a layer separation operation. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 447 mg of methyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09447090B2 |
|---|
| Quelldatensatz | uspto-grants-2016_09 |
|---|
| ORD ID | ord-bfc183d973b3464fa90f16ef138d3c7f |
|---|
| Quellennotiz | uspto-grants-2016_09 |
|---|