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Acrylic Acid → N-acryloxyethylundecylamide

HRID 1066954
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인쇄 미리보기

반응식

HRID 1066954 반응식
[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([C:17]1[O:18][CH2:19][CH2:20][N:21]=1)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]C>C(OCC)C>[C:1]([O:5][CH2:19][CH2:20][NH:21][C:17](=[O:18])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])(=[O:4])[CH:2]=[CH2:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6581Acrylic AcidHCID 3470762-Undecyl-2-oxazoline

생성물 1

HCID 21196858N-acryloxyethylundecylamide

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

반응 조건

온도
80 °C

실험 절차

51.99 g acrylic acid and 0.3 g BHT were heated in a round-bottom flask to 80° C. Under stirring, 81.3 g molten undecyl oxazoline was slowly added during 1 hour maintaining the reaction temperature at 80° C . After stirring for another hour at 80° C. the reaction mixture was poured into 200 ml diethyl ether and washed with water, twice with a 10% sodium bicarbonate solution and twice with water. After drying on magnesium sulfate, filtration and evaporation in vacuo of the solvent 100.5 g of N-acryloxyethylundecylamide was obtained.

후처리

  1. stirringAfter stirring for another hour at 80° C. the reaction mixture
  2. washwashed with water, twice with a 10% sodium bicarbonate solution and twice with water
  3. dry with materialAfter drying on magnesium sulfate, filtration and evaporation in vacuo of the solvent 100.5 g of N-acryloxyethylundecylamide
  4. customwas obtained

출처 및 근거

ORD 기록
ord-573863e9e3d548579447ef70e66bef81
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06245829B1

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