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Phthalic Anhydride → HCID 21544573, 화합물

HRID 1606778
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HRID 1606778 반응식
[CH:1]12[O:8][CH:5]([CH2:6][CH2:7]1)[CH2:4][NH:3][CH2:2]2.[C:9]1(=[O:19])[O:14][C:12](=[O:13])[C:11]2=[CH:15][CH:16]=[CH:17][CH:18]=[C:10]12>C1C=CC=CC=1>[C:12]([C:11]1[CH:15]=[CH:16][CH:17]=[CH:18][C:10]=1[C:9]([N:3]1[CH2:2][CH:1]2[O:8][CH:5]([CH2:6][CH2:7]2)[CH2:4]1)=[O:19])([OH:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6811Phthalic AnhydrideHCID 120692318-Oxa-3-azabicyclo[3.2.1]octane

생성물 1

HCID 21544573HCID 21544573, 화합물

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

A solution of 11.3 grams (0.1 mole) 8-oxa-3-azabicyclo (3.2.1)octane in 20 ml of benzene was added to a suspension of 14.8 grams (0.1 mole) of phthalic anhydride in 50 ml of benzene at 8° C. The reaction mixture was stirred for 1 hour and then left overnight at room temperature. The product, 20.0 grams which separated, was filtered off and recrystallized from benzene ethanol. The product represented by formula (X) had a melting point of 149°-150.5° C.

후처리

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  • waitleft overnight at room temperature
  • customThe product, 20.0 grams which separated
  • filtrationwas filtered off
  • customrecrystallized from benzene ethanol
  • 출처 및 근거

    ORD 기록
    ord-9fe9fbd11ee34de787a67fa9aa9460ff
    출처 데이터셋
    uspto-grants-1976_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03953596

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