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Acetic Anhydride → 4-[1-Acetoxy-6-(2-pyridyl)hexyl]-2-trimethylsilylfuran

HRID 654937
ノート
印刷プレビュー

反応式

HRID 654937 の反応式
C([Li])(C)(C)C.Br[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][N:13]=1.[CH3:18][Si:19]([CH3:28])([CH3:27])[C:20]1[O:24][CH:23]=[C:22]([CH:25]=[O:26])[CH:21]=1.[C:29](OC(=O)C)(=[O:31])[CH3:30]>CCCCC.O1CCCC1>[C:29]([O:26][CH:25]([C:22]1[CH:21]=[C:20]([Si:19]([CH3:28])([CH3:27])[CH3:18])[O:24][CH:23]=1)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][N:13]=1)(=[O:31])[CH3:30]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 7918Acetic AnhydrideHCID 156632515-(Trimethylsilyl)furan-3-carbaldehydeHCID 198859142-(5-Bromopentyl)pyridineHCID 178418306HCID 178418306、化合物

生成物 1

HCID 157233774-[1-Acetoxy-6-(2-pyridyl)hexyl]-2-trimethylsilylfuran

試薬・触媒・溶媒 2

HCID 8003Pentane
溶媒
HCID 8028Tetrahydrofuran溶媒2 回

実験手順

tert-Butyl lithium (a 1.7M solution in pentane; 2.4 ml, 4.14 mmol) was added dropwise to a solution of 2-(5-bromopentyl)pyridine (472.3 mg, 2.07 mmol) in tetrahydrofuran (7 ml) at -78° under argon. After 1 hour, a solution of 5-trimethylsilyl-3-furaldehyde (348 mg, 2.07 mmol) in tetrahydrofuran (1 ml) was added, followed by acetic anhydride (0.59 ml, 6.21 mmol) after 2 hours. The mixture was allowed to warm to room temperature and quenched with water (after 22 hours). Extraction (ethyl ether) and evaporation of the dried (magnesium sulphate) extracts gave an oil, which was flash chromatographed on silica using 40% ethyl acetate/hexane. Fractions with Rf of about 0.25 on evaporation gave the title silyfuran as a light brown oil.

後処理

  1. customquenched with water (after 22 hours)
  2. extractionExtraction (ethyl ether) and evaporation of the
  3. dry with materialdried (magnesium sulphate)
  4. customextracts gave an oil, which
  5. customchromatographed on silica using 40% ethyl acetate/hexane
  6. customFractions with Rf of about 0.25 on evaporation
  7. customgave the title silyfuran as a light brown oil

出典と根拠

ORDレコード
ord-8ccddbc0901546138fe1e1a012ad93b8
出典データセット
uspto-grants-1992_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05134128

反応ノート

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