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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278461Erstellt: 24. Oktober 2026

Triethylamine → Ethyl (alphaR)-alpha-[(methylsulfonyl)oxy]benzenebutanoate

https://huagongshe.com/de/reaction/278461

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
EduktEthyl (R)-2-hydroxy-4-phenylbutyrateHCID 2733848—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl (alphaR)-alpha-[(methylsulfonyl)oxy]benzenebutanoateHCID 1479447099,6%

Reaktionsschritte

Triethylamine (583 mg) was added dropwise to a stirred mixture of ethyl (R)-2-hydroxy-4-phenylbutyrate (1.0 g) and methanesulfonyl chloride (660 mg) in dichloromethane (10 ml) at ice-bath temperature. After 40 minutes, the reaction mixture was partitioned between dichloromethane and water. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated in vacuo to give ethyl (R)-2-methylsulfonyloxy-4-phenylbutyrate (1.37 g) as an oil. This material was used immediately without further purification. NaH (60% in mineral oil, 192 mg) was added to a solution of 4-imidazolecarboxamide (534 mg) in DMF (8 ml) at room temperature. The reaction mixture was stirred for 30 minutes. The methanesulfonate prepared above was added and the resulting mixture was stirred for 3 hours at 60° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06359145B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-8533e20906c04d8ca834359ae849788c
Quellennotizuspto-grants-2002_03