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Acetic Anhydride → HCID 19848591, 화합물

HRID 1608217
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인쇄 미리보기

반응식

HRID 1608217 반응식
[OH:1][CH2:2][CH2:3][CH:4]1[O:9][CH2:8][CH2:7][N:6]([CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:5]1.C(N(CC)CC)C.[C:24](OC(=O)C)(=[O:26])[CH3:25]>C(OCC)(=O)C>[C:24]([O:1][CH2:2][CH2:3][CH:4]1[O:9][CH2:8][CH2:7][N:6]([CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:5]1)(=[O:26])[CH3:25]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7918Acetic AnhydrideHCID 8471TriethylamineHCID 146525912-(4-Benzylmorpholin-2-yl)ethan-1-ol

생성물 1

HCID 19848591HCID 19848591, 화합물

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

반응 조건

온도
25 °C

실험 절차

To a mixture of 2-(2-hydroxyethyl)-4-benzylmorpholine (27.7 g), triethylamine (28 ml), and ethyl acetate (100 ml) is dropwise added acetic anhydride (17.8 ml). The reaction mixture is stirred at 25° C. for 1 hour and evaporated under reduced pressure. The residue is dissolved in chloroform and chromatographed on silica gel. Fractions containing the title compound are pooled and evaporated to give the title compound (29.1 g) as an oil.

후처리

  1. customevaporated under reduced pressure
  2. dissolutionThe residue is dissolved in chloroform
  3. customchromatographed on silica gel
  4. additionFractions containing the title compound
  5. customevaporated

출처 및 근거

ORD 기록
ord-b3b31a3f49f8428eafef6c5ad638ed59
출처 데이터셋
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04870074

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