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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30525Erstellt: 24. Oktober 2026

Isobutyric Acid → Benzyl 3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-5-Methyl-Hexanoate

https://huagongshe.com/de/reaction/30525

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsobutyric AcidHCID 6590—
Edukt4-MethylmorpholineHCID 7972—
EduktBenzyl 3-{[(alpha-Chloroethoxy)carbonyl]aminomethyl}-5-Methyl-HexanoateHCID 21113521—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzyl 3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-5-Methyl-HexanoateHCID 66887904—

Reaktionsschritte

A solution of (40) (0.53 g, 1.50 mmol) in isobutyric acid (1 mL) was added to a mixture of isobutyric acid (0.96 mL, 10.8 mmol) and N-methylmorpholine (1.14 mL, 10.4 mmol) at room temperature. The resulting reaction mixture was stirred at room temperature for 48 h. The reaction mixture was diluted with dichloromethane, washed successively with water, 10% aqueous NaHCO3 solution and brine, then dried over anhydrous Na2SO4. After filtration and removal of the solvent in vacuo, the residue was purified by flash chromatography on silica gel, eluting with 5% ethyl acetate in hexane to afford the title compound (41) as a mixture of two diastereomers (400 mg, 66%). 1H—NMR (CDCl3, 400 MHz): δ 0.85 (m, 6H), 1.14 (m, 8H), 1.44 (m, 3H), 1.62 (m, 1H), 2.13 (m, 1H), 2.32 (m, 2H), 2.51 (m, 1H), 3.06 (m, 1H), 3.24 (m, 1H) 4.95 (m, 1H), 5.10 (s, 2H), 6.76 (q, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423169B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-7215531b15434df8beee00b176cccbb1
Quellennotizuspto-grants-2008_09