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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64432Erstellt: 25. Oktober 2026

Triethylamine → Methyl (S)-3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate

https://huagongshe.com/reaction/64432

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1,3-Bis(diphenylphosphino)propaneHCID 81219—
Edukt(S)-N-Boc-1-(3-bromophenyl)ethylamineHCID 56971804—
EduktHCID 178418416HCID 178418416—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl (S)-3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoateHCID 86713444151,2%

Reaktionsschritte

To 820 mg of tert-butyl[(1S)-1-(3-bromophenyl)ethyl]carbamate were added 113 mg of 1,3-bis(diphenylphosphino)propane, 62 mg of palladium acetate, 0.84 ml of triethylamine, 8 ml of DMF, and 12 ml of methanol, followed by stirring at room temperature for 1 hour. While stirring at room temperature, carbon monooxide was intaken for 10 minutes, followed by stirring at 80° C. overnight under a carbon monooxide atmosphere. 113 mg of 1,3-bis(diphenylphosphino)propane and 62 mg of palladium acetate were added thereto, followed by stirring at 80° C. overnight. To the reaction mixture were added water 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 577 mg of methyl 3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}benzoate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447090B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-883b23c1c5814e0b8408008803b23aa6
Quellennotizuspto-grants-2016_09