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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 742064Erstellt: 25. Oktober 2026

Heptane → methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate

https://huagongshe.com/reaction/742064

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHeptaneHCID 8900—
EduktThionyl ChlorideHCID 24386—
EduktN-[4-methoxybenzenesulfonyl]-(D)-valineHCID 1133588—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
Produktmethyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoateHCID 10946547—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To a solution of N-[4-methoxybenzenesulfonyl]-(D)-valine (8369 g, 29.13 mol) in methanol (30 L) at 5° C. is added thionyl chloride (2176 mL, 29.7 mol) over 2.5 hours. After stirring for 3 hours at 5° C., the reaction is stirred for 36 hours at room temperature. Most of the solvent is evaporated, and the crude product is dissolved in toluene (80 L). The toluene layer is then washed with water (20 L), saturated sodium bicarbonate (20 L), water again (20 L), 2N hydrochloric acid (20 L), brine (20 L), dried (Na2SO4), and the solvent is evaporated. The solid obtained is dissolved in ethyl acetate (8 L) and heptane (16 L) is added to induce crystallization. The precipitated product is collected by filtration to provide methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05552419
Quelldatensatzuspto-grants-1996_09
ORD IDord-50f2adec32c14d05959b81a4942581fc
Quellennotizuspto-grants-1996_09