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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Eduktmethyl 3-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]benzoateHCID 90072367—
EduktHCID 178443585HCID 178443585—
EduktHCID 178467792HCID 178467792—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produktmethyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447090B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-bfc183d973b3464fa90f16ef138d3c7f
Quellennotizuspto-grants-2016_09