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2-Butyne-1,4-diol → (4-Hydroxy-but-2-ynyloxy)-acetonitrile

HRID 2052971
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HRID 2052971 반응식
[H-].[Na+].[CH2:3]([OH:8])[C:4]#[C:5][CH2:6][OH:7].Br[CH2:10][C:11]#[N:12]>C1COCC1>[OH:7][CH2:6][C:5]#[C:4][CH2:3][O:8][CH2:10][C:11]#[N:12]
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참가 물질

5

반응물 3

HCID 80662-Butyne-1,4-diolHCID 11534BromoacetonitrileHCID 24758Sodium hydride

생성물 1

HCID 86012515(4-Hydroxy-but-2-ynyloxy)-acetonitrile수율 29%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Sodium hydride (60% dispersion in oil, 7.5 g, 188 mmol) was added to a solution of 2-butyne-1,4-diol (16.1 g, 187 mmol) in THF (150 mL) at 0° C. under nitrogen. After 1 h at 0° C., bromoacetonitrile (8.33 mL, 120 mmol) was added slowly and the reaction was allowed to warm to rt. After 22 h at rt, the reaction was quenched with 1 N HCl (150 mL) and extracted with EtOAc (3×150 mL). The combined extracts were washed with brine (150 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient) afforded 4.35 μg (29%) of (4-hydroxy-but-2-ynyloxy)-acetonitrile.

후처리

  1. waitAfter 22 h at rt
  2. customthe reaction was quenched with 1 N HCl (150 mL)
  3. extractionextracted with EtOAc (3×150 mL)
  4. washThe combined extracts were washed with brine (150 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customPurification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient)

출처 및 근거

ORD 기록
ord-640f5b5899244b619ab9765acc232bb9
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07326716B2

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