KR960701180A - 아세토글리세리드 지방의 합성(synthesis of acetoglyceride fats) - Google Patents

아세토글리세리드 지방의 합성(synthesis of acetoglyceride fats) Download PDF

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KR960701180A
KR960701180A KR1019950703208A KR19950703208A KR960701180A KR 960701180 A KR960701180 A KR 960701180A KR 1019950703208 A KR1019950703208 A KR 1019950703208A KR 19950703208 A KR19950703208 A KR 19950703208A KR 960701180 A KR960701180 A KR 960701180A
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South Korea
Prior art keywords
triglycerides
triacetin
catalyst
potassium
solvent
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KR1019950703208A
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English (en)
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KR100286955B1 (ko
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펠로소 투리듀 에이
디. 로덴 알랜
엘. 볼트 길버트
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로버트 게이, 드 브리에스
나비스코, 인코포레이티드
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    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
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  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

아세토글리세리드는 용매없이 제조된다. C2내지 C10의 포화 산 잔기를 반응 혼합물에 가함으로서 긴 C10내지 C22긴 사슬 지방산잔기를 포함하는 트리글리세리드 및 트리아세틴 사이의 단일상 에스테르화시켜 제조된다. 긴 사슬 잔기는 상호 에스테르화반응의 전후에 수소화될 수 있다. 일 실시예에 있어서, C3내지 C10의 트리글리세리드는 트리프로피오닌, 트리부티린 또는 이들의 혼합물이며, 이들은 C8내지 C10잔기를 포함하는 트리글리세리드이고, 트리프로피온 및/또는 트리부티린 혼합물이다. 바람직한 실시예에 있어서, 트리아세틴 및 C3내지 C10의 트리글리세리드에 대한 C16내지 C22의 트리글리세리드의 몰비율은 1:1 내지 1:15, 바람직하게는 1:3 내지 1:12이며, 고온이 사용된다. 이러한 공정은 촉매사용을 줄이고 높은 전단 혼합이 필요없게 하고 반응시간을 단축시키며, 정제 단계를 간단하게 한다.

Description

아세토글리세리드 지방의 합성(SYNTHESIS OF ACETOGLYCERIDE FATS)
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (10)

  1. 촉매 존재하에서 단일상으로 C3내지 C10의 포화 산 잔기를 포함하는 트리글리세리드 및 트리아세틴에 의해 C16내지 C22긴 지방산 잔기를 포함하는 트리글리세리드를 포함하는 C16내지 C22의 지방산 잔기 및 아세틸 잔기를 상호에스테르화하는 단계를 포함하는 용매 불사용 트리글리세리드 합성 방법.
  2. 촉매 및 용매 존재하에서 완전히 수소화된 오일을 트리아세틴으로 상호에스테르화하는 방법에 있어서, C3내지 C10을 포함하는 트리글리세리드가 반응 혼합물에 가해지고 반응이 용매없이 유도되는 것을 특징으로 하는 수소화된 오일의 상호에스테르화 방법.
  3. 알칼리 금속 알콕시화물 촉매 및 용매의 존재하에서, 120℃미만의 온도로 반응 혼합물을 교반 및 가열시킴으로서 완전히 수소화된 오일과 트리아세틴을 상호에스테르화시키는 방법에 있어서, 트리프로피오닌을 반응혼합물에 가하여 반응을 용매없이 단일상으로 행하는 것을 특징으로 하는 수소화된 오일과 트리아세틴을 상호 에스테르화시키는 방법.
  4. 제1항, 2항 또는 3항에 있어서, C3내지 C10의 산 잔기를 포함하는 트리아세틴 및 트리글리세린등 대한 C16내지 C22의지방산 잔기를 포함하는 트리글리세리드의 반응성 몰비율이 1:1 내지 1:15의 비율인 것을 특징으로 하는 방법.
  5. 제4항에 있어서, 비율이 1:3 내지 1:12인 것을 특징으로 하는 방법.
  6. 제1항, 2항 또는 3항에 있어서, C3내지 C10포화산 잔기를 포함하는 트리글리세리드는 트리프로피오닌 및 트리부티린 혼합물로 이루어진 그룹으로부터 선택되는 포화 C8내지 C10의 산 잔기 및 트리글리세리드를 포함하는 트리글리세리드 혼합물인 것을 특징으로 하는 방법.
  7. 제1,2 또는 3항에 있어서, C3내지 C10의 포화산 잔기를 포함하는 트리글리세리드는 트리프로피오닌 및 트리부티린 혼합물로 이루어진 그룹으로부터 선택되는 것을 특징으로 하는 방법.
  8. 제1,2항,또는 3항에 있어서, 촉매는 알칼리 금속 알콕시화물, 나트륨, 칼륨 및 나트륨/칼륨 합금으로 이루어진 그룹으로부터 선택되는 것을 특징으로 하는 방법.
  9. 제8항에 있어서, 촉매가 메톡시화 칼륨, 메톡시화 리튬, 에톡시화 나트륨, 에톡시화칼륨, 에톡시화 리튬, 트로폭시화 나트륨, 트로폭시화 칼륨, 트로폭시화 리튬, 부톡시화 나트륨, 부톡시화 칼륨, 부톡시화 리튬으로 이루어진 그룹으로 부터 선택되는 것을 특징으로 하는 방법.
  10. 제1항, 2항 또는 3항에 있어서, 반응이 120℃ 냐자 150℃에서 수행되는 것을 특징으로 하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019950703208A 1993-02-03 1994-02-03 아세토글리세리드 지방의 합성방법 KR100286955B1 (ko)

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US08/012,712 US5434278A (en) 1989-09-20 1993-02-03 Synthesis of acetoglyceride fats
US08/012,712 1993-02-03
US8/012712 1993-02-03
PCT/US1994/001145 WO1994018290A1 (en) 1993-02-03 1994-02-03 Synthesis of acetoglyceride fats

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JPH08506607A (ja) 1996-07-16
CA2153411A1 (en) 1994-08-18
NO953043L (no) 1995-09-29
FI953685A0 (fi) 1995-08-02
NO953043D0 (no) 1995-08-02
TW408107B (en) 2000-10-11
NZ261791A (en) 1997-03-24
EP0682689A4 (en) 1996-02-28
US5434278A (en) 1995-07-18
WO1994018290A1 (en) 1994-08-18
AU6099894A (en) 1994-08-29
AU670187B2 (en) 1996-07-04
KR100286955B1 (ko) 2001-04-16
FI953685A (fi) 1995-08-30

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