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Sodium borohydride → 6-Chloro-3,4-dihydro-4-hydroxy-spiro[2H-1-benzopyran-2,1'-cyclobutane]

HRID 1175759
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인쇄 미리보기

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HRID 1175759 반응식
[BH4-].[Na+].[Cl:3][C:4]1[CH:5]=[CH:6][C:7]2[O:15][C:11]3([CH2:14][CH2:13][CH2:12]3)[CH2:10][C:9](=[O:16])[C:8]=2[CH:17]=1>CO>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]2[O:15][C:11]3([CH2:12][CH2:13][CH2:14]3)[CH2:10][CH:9]([OH:16])[C:8]=2[CH:17]=1
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 667465206-Chlorospiro[chroman-2,1'-cyclobutan]-4-one

생성물 1

HCID 667463666-Chloro-3,4-dihydro-4-hydroxy-spiro[2H-1-benzopyran-2,1'-cyclobutane]

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
0 °C

실험 절차

Sodium borohydride (40 mmol) was added to a solution of 6-Chloro-3,4-dihydro-4-oxo-spiro[2H-1-benzopyran-2,1′-cyclobutane] (10 mmol) in methanol (10 ml). at about 0° C. and the reaction mixture was stirred at room temperature for about 2 h and compound was extracted in ethyl acetate. Organic layer was washed with water, brine and separated. It was then dried on anhydrous sodium sulfate and concentrated to afford the desired product as a white solid.

후처리

  1. extractioncompound was extracted in ethyl acetate
  2. washOrganic layer was washed with water, brine
  3. customseparated
  4. dry with materialIt was then dried on anhydrous sodium sulfate
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-83e3f64ff7d3473c9a4e37f6fbdd4e0d
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07842703B2

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