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Thallous nitrate → 3-methoxy-1,2,3,4-tetrahydro-5H-benzocyclohepten-6-one

HRID 274048
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HRID 274048 반응식
[N+]([O-])([O-])=[O:2].[Tl+].[CH2:6]=[C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([O:17][CH3:18])[CH:15]=2)[CH2:10][CH2:9][CH2:8]1>CO.C(Cl)(Cl)Cl>[CH3:18][O:17][CH:14]1[CH2:13][CH2:12][C:11]2=[CH:10][CH:9]=[CH:8][C:6](=[O:2])[CH2:7][CH:16]2[CH2:15]1
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참가 물질

5

반응물 2

HCID 24937Thallous nitrateHCID 109650271-Methylene-7-methoxy-1,2,3,4-tetrahydronaphthalene

생성물 1

HCID 676857843-methoxy-1,2,3,4-tetrahydro-5H-benzocyclohepten-6-one수율 70.7%

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 6212Chloroform용매

실험 절차

To a solution of thallium nitrate (2.4 g) in methanol (24 ml) was added 1-methylene-7-methoxy-1,2,3,4-tetrahydronaphthalene (1.0 g) in methanol (7 ml) in one portion. The mixture was stirred for 1 minute and diluted with chloroform (24 ml). The resulting precipitate was filtered off and the filtrate was washed with saturated aqueous sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by column chromatography on silica gel (elution; 8:1, n-hexane-ethyl acetate) to give 3-methoxy-1,2,3,4-tetrahydro-5H-benzocyclohepten-6-one (0.78 g).

후처리

  1. filtrationThe resulting precipitate was filtered off
  2. washthe filtrate was washed with saturated aqueous sodium bicarbonate and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography on silica gel (elution; 8:1, n-hexane-ethyl acetate)

출처 및 근거

ORD 기록
ord-5c6816d4a0254c81bc22b5e2cf0e7d37
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05387710

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