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Sodium borohydride → HCID 53944516, 화합물

HRID 726177
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HRID 726177 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:14]=1[S:13][CH2:12][CH2:11][C:10]2=[O:15])=[O:4].[BH4-].[Na+]>C(O)C>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:14]=1[S:13][CH2:12][CH2:11][CH:10]2[OH:15])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 130039219HCID 130039219, 화합물

생성물 1

HCID 53944516HCID 53944516, 화합물수율 99%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Methylthiochroman-4-one-8-carboxylate (0.500 g, 2.25mmol) was dissolved with stirring in ethanol (20 ml) and treated with sodium borohydride (0.085 g, 2.25 mmol). After 1 h, the reaction mixture was evaporated under reduced pressure and the residue partitioned between ethyl acetate and water. The aqueous layer was then extracted with ethyl acetate (1 x) and the combined organic layers were dried (Na2SO4) and evaporated under reduced pressure to give a yellow oil, which was purified by silica-gel chromatography (1:1 Pentane:EtOAc as eluant) to give the title compound as a colourless oil (0.499 g, 99%)

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후처리

  1. customthe reaction mixture was evaporated under reduced pressure
  2. customthe residue partitioned between ethyl acetate and water
  3. extractionThe aqueous layer was then extracted with ethyl acetate (1 x)
  4. dry with materialthe combined organic layers were dried (Na2SO4)
  5. customevaporated under reduced pressure
  6. customto give a yellow oil, which
  7. customwas purified by silica-gel chromatography (1:1 Pentane:EtOAc as eluant)

출처 및 근거

ORD 기록
ord-5640b55abd2342b98d780d8ad7459911
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05708174

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