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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 964330Erstellt: 25. Oktober 2026

Dicyclohexylcarbodiimide → Acetyl-3-phenylthiopropionate

https://huagongshe.com/reaction/964330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
EduktMenthoneHCID 26447—
EduktBoronHCID 5462311—
Eduktalpha-Methoxy-alpha-trifluoromethylphenylacetic acid, (-)-HCID 6992788—
Edukttertbutyl 3(R)-benzoylamino-2(S)-hydroxy-3-phenylthiopropionateHCID 86752783—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktAcetyl-3-phenylthiopropionateHCID 54171142—

Reaktionsschritte

A pure sample of tertbutyl 3(R)-benzoylamino-2(S)-hydroxy-3-phenylthiopropionate was obtained via the same reaction sequence, but using the boron reagent di{[(1S,2S,5R)-2-isopropyl-5-methylcyclohex-1-yl]-methyl}boron bromide, derived from (-)menthone. Compound tertbutyl 3(R)-benzoylamino-2(S)-hydroxy-3-phenylthiopropionate was treated with excess (S)-(-)-α-methoxy-α-(trifluoromethyl) phenylacetic acid in dichloromethane in the presence of 1,3-dicyclohexylcarbodiimide (DCC) and catalytic 4-dimethylaminopyridine (DMAP). The Mosher derivative tertbutyl 3(R)-benzoylamino-2(S)-O-[(S)-α-methoxy-α-trifluoromethyl)phenyl]acetyl-3-phenylthiopropionate was obtained:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05767282
Quelldatensatzuspto-grants-1998_06
ORD IDord-161ad47b2c054bd398e35e0a3f26f471
Quellennotizuspto-grants-1998_06