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HCID 12262631, 화합물 → 3-Methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-one

HRID 274079
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HRID 274079 반응식
N[CH2:2][C:3]1([OH:15])[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=2)[CH2:6][CH2:5][CH2:4]1.N([O-])=O.[Na+]>C(O)(=O)C.O>[CH3:14][O:13][C:10]1[CH:9]=[CH:8][C:7]2[CH2:6][CH2:5][CH2:4][C:3](=[O:15])[CH2:2][C:12]=2[CH:11]=1
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참가 물질

5

반응물 2

HCID 12262631HCID 12262631, 화합물HCID 23668193Sodium Nitrite

생성물 1

HCID 105595743-Methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-one수율 76.8%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

To a solution of 1-aminomethyl-7-methoxy-1,2,3,4-tetrahydro-1-naphthalenol (27.50 g) in 10% aqueous acetic acid solution (250 ml) was added dropwise a solution of sodium nitrite (10.07 g) in water (61 ml) at 8° C.~9° C. The reaction mixture was stirred for 2 hours at the same temperature. The resulting precipitates were collected by filtration. The precipitates were dissolved in ethyl acetate. The solution was dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography (silica gel, n-hexane:ethyl acetate:chloroform=5:1:3) to give 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-one (19.39 g) as a white powder.

후처리

  1. customThe resulting precipitates
  2. filtrationwere collected by filtration
  3. dissolutionThe precipitates were dissolved in ethyl acetate
  4. dry with materialThe solution was dried over magnesium sulfate
  5. customevaporated in vacuo
  6. customThe residue was purified by column chromatography (silica gel, n-hexane:ethyl acetate:chloroform=5:1:3)

출처 및 근거

ORD 기록
ord-9dda68e7336240aaa16a72cc41678acc
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05387710

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