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HRID 39251Erstellt: 23. Oktober 2026

Butyric Acid → 2,2-Dimethoxyethyl butyrate

https://huagongshe.com/de/reaction/39251

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyric AcidHCID 264—
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukt2-Bromo-1,1-dimethoxyethaneHCID 81672—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelAcetonitrileHCID 6342—
Produkt2,2-Dimethoxyethyl butyrateHCID 1136730078%

Reaktionsbedingungen

Temperatur134 °C

Reaktionsschritte

A mixture of butyric acid (1.0 g, 11.35 mmol), bromoacetaldehyde dimethyl acetal (2.25 mL, 19.13 mmol), tetrabutylammonium bromide (1.83 g, 5.67 mmol) and K2CO3 (1.56 g, 11.35 mmol) in 10 mL of anhydrous CH3CN was stirred at 134° C. for 16 h in a sealed tube. It was cooled to room temperature, water was added and the mixture was extracted with Et2O (3×120 mL). The combined organic phases were washed with saturated NaCl (2×60 mL), dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel using 20-30% ethyl acetate/hexanes to give the product 43a (1.56 g, 78%). 1H NMR (400 MHz, CDCl3) δ 0.90 (t, J=7.43 Hz, 3H), 1.60 (sextet, J=7.43, 7.04 Hz, 2H), 2.24 (t, J=7.04 Hz, 2H), 3.36 (s, 6H), 4.08 (d, J=5.3 Hz, 2H), 4.54 (t, J=5.3 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524691B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-5d5ededb485a4de2877448b0b3b2ec91
Quellennotizuspto-grants-2013_09