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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39251생성일: 2026년 10월 23일

Butyric Acid → 2,2-Dimethoxyethyl butyrate

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

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참여 물질

역할이름HCID투입량
반응물Butyric AcidHCID 264—
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물2-Bromo-1,1-dimethoxyethaneHCID 81672—
촉매Tetrabutylammonium BromideHCID 74236—
용매AcetonitrileHCID 6342—
생성물2,2-Dimethoxyethyl butyrateHCID 1136730078%

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온도134 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524691B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5d5ededb485a4de2877448b0b3b2ec91
출처 메모uspto-grants-2013_09