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Pivalaldehyde → HCID 24873309, 화합물

HRID 222844
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HRID 222844 반응식
[Br:1][C:2]([F:16])([F:15])[C:3]#[C:4][Si](C(C)C)(C(C)C)C(C)C.[CH3:17][C:18]([CH3:22])([CH3:21])[CH:19]=[O:20]>C1COCC1.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>[Br:1][C:2]([F:15])([F:16])[C:3]#[C:4][CH:19]([OH:20])[C:18]([CH3:22])([CH3:21])[CH3:17]
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참가 물질

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HCID 12417PivalaldehydeHCID 10990566(3-Bromo-3,3-difluoroprop-1-yn-1-yl)tris(propan-2-yl)silane

생성물 1

HCID 24873309HCID 24873309, 화합물

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 2724141Tetrabutylammonium Fluoride용매

실험 절차

To a solution of (3-bromo-3,3-difluoro-prop-1-ynyl)-triisopropyl-silane (156 mg, 0.5 mmol) and 2,2-dimethyl-propionaldehyde (52 mg, 0.6 mmol) in THF (5 mL), TBAF (1M, 0.75 mL) was added dropwise at −90° C. After the addition was completed, the reaction mixture was stirred for 0.5 hour and quenched saturated aq. NH4Cl. The mixture was extracted with ether (20 mL×3) and washed with water (20 mL×2). After drying over Na2SO4 the solvent was removed and the product was purified by silica gel chromatography (AcOEt:hexane=1:20) to afford the title compound as a colorless liquid. 1H NMR (500 MHz, CDCl3) δ 4.08-4.09 (m, 1H), 1.83 (d, J=6.0 Hz, 1H), 0.965 (s, 9H).

후처리

  1. additionAfter the addition
  2. customquenched saturated aq. NH4Cl
  3. extractionThe mixture was extracted with ether (20 mL×3)
  4. washwashed with water (20 mL×2)
  5. dry with materialAfter drying over Na2SO4 the solvent
  6. customwas removed
  7. customthe product was purified by silica gel chromatography (AcOEt:hexane=1:20)

출처 및 근거

ORD 기록
ord-bb04b3753cb84583a4818fadba881389
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08207381B2

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