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Water → 6-t-Butyldimethylsilyloxy-6-(2-naphthyl)hexanal

HRID 1182503
ノート
印刷プレビュー

反応式

HRID 1182503 の反応式
[Si:1]([O:8][CH:9]([C:16]1[CH:25]=[CH:24][C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=1)[CH2:10][CH2:11][CH2:12][CH2:13][CH:14]=C)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].O.C(=O)(O)[O-:28].[Na+].I([O-])(=O)(=O)=O.[Na+]>C(O)(C)(C)C.[Os](=O)(=O)(=O)=O>[Si:1]([O:8][CH:9]([C:16]1[CH:25]=[CH:24][C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=1)[CH2:10][CH2:11][CH2:12][CH2:13][CH:14]=[O:28])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]
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 962WaterHCID 516892Sodium BicarbonateHCID 23072469O-(t-Butyldimethylsilyl)-1-(2-naphthyl)-6-heptenolHCID 23667635Sodium periodate

生成物 1

HCID 109482766-t-Butyldimethylsilyloxy-6-(2-naphthyl)hexanal収率 91%

試薬・触媒・溶媒 2

HCID 30318
Osmium Tetroxide
触媒
HCID 6386tert-Butanol溶媒

実験手順

To a solution of alkene 182 (1.05 g, 3.23 mmol) in t-butyl alcohol (50 mL) were successively added water (10 mL), solid sodium bicarbonate (2.71 g, 32.3 mmol), sodium periodate (4.15 g, 19.38 mmol), and osmium tetroxide (8 mg, 0.032 mmol). The mixture turned light brown and a precipitate formed in large amount, making magnetic stirring impossible so the mixture was shaken by hand every 10 minutes for 3.5 hours and the brownish color almost disappeared. The reaction was quenched with a 10% aqueous solution of sodium thiosulfate. After 30 minutes, the white precipitate was filtered off and rinsed with diethyl ether. The filtrate was concentrated in vacuo. The residue was partitioned between diethyl ether and water. The aqueous layer was extracted (2×50 mL) with diethyl ether. The combined organic layers were washed successively with a 10% aqueous solution of sodium thiosulfate, water and brine, dried (MgSO4), and concentrated in vacuo, yielding the title compound 183 as a crude oil in 91% yield (1.05 g). 1H NMR: (300 MHz, CDCl3) δ: 9.73 (t, J=1.9 Hz, 1H), 7.83-7.78 (m, 3H), 7.69 (s, 1H), 7.49-7.43 (m, 3H), 4.80 (t, J=6.9 Hz, 1H), 2.39 (td, J=7.1, 1.6 Hz, 2H), 1.81-1.55 (m, 4H), 1.43-1.25 (m, 2H) 0.90 (s, 9H), 0.04 (s, 3H), −0.15 (s, 3H). MS (ESI) 225 (M+1-TBSO).

後処理

  1. customa precipitate formed in large amount
  2. stirringwas shaken by hand every 10 minutes for 3.5 hours
  3. customThe reaction was quenched with a 10% aqueous solution of sodium thiosulfate
  4. filtrationthe white precipitate was filtered off
  5. washrinsed with diethyl ether
  6. concentrationThe filtrate was concentrated in vacuo
  7. customThe residue was partitioned between diethyl ether and water
  8. extractionThe aqueous layer was extracted (2×50 mL) with diethyl ether
  9. washThe combined organic layers were washed successively with a 10% aqueous solution of sodium thiosulfate, water and brine
  10. dry with materialdried (MgSO4)
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-2a586bba723743ed9aa38a7045dec2a5
出典データセット
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07288567B2

反応ノート

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