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2-Methylbenzaldehyde → tert-Butyl(dimethyl){[3-(2-methylbenzylidene)-1-cyclohepten-1-yl]oxy}silane

HRID 989262
ノート
印刷プレビュー

反応式

HRID 989262 の反応式
[C:1]1(=[O:8])[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O([Si:36]([C:39]([CH3:42])([CH3:41])[CH3:40])([CH3:38])[CH3:37])S(C(F)(F)F)(=O)=O.[Li]CCCC.CCCCCC.[CH3:54][C:55]1[CH:62]=[CH:61][CH:60]=[CH:59][C:56]=1[CH:57]=O>C1COCC1>[C:39]([Si:36]([CH3:38])([CH3:37])[O:8][C:1]1[CH2:7][CH2:6][CH2:5][CH2:4][C:3](=[CH:54][C:55]2[CH:62]=[CH:61][CH:60]=[CH:59][C:56]=2[CH3:57])[CH:2]=1)([CH3:42])([CH3:41])[CH3:40]
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 5

HCID 107222-MethylbenzaldehydeHCID 11776TriphenylphosphineHCID 707232-Cyclohepten-1-oneHCID 123564tert-Butyldimethylsilyl trifluoromethanesulphonateHCID 178418244HCID 178418244、化合物

生成物 1

HCID 69965728tert-Butyl(dimethyl){[3-(2-methylbenzylidene)-1-cyclohepten-1-yl]oxy}silane

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of cycloheptenone (71.7 mmol) in 220 ml of anhydrous THF there are added, in succession, triphenylphosphine (72.6 mmol) and then, dropwise, tert-butyldimethylsilyl triflate (72.3 mmol), and the whole is stirred at room temperature for 1 hour 30 minutes. The mixture is then brought to −78° C., and a solution of nBuLi/hexane (72 mmol) is added slowly, followed 30 minutes later by 2-methylbenzaldehyde (72.03 mmol). The whole is stirred at that temperature for 30 minutes, and then with the temperature gradually returning to room temperature. After 2 hours 30 minutes, the reaction mixture is precipitated from 2.5 liters of petroleum ether and filtered, and the filtrate is concentrated to dryness. The title product is purified by chromatography over silica gel (100% heptane).

後処理

  1. customis then brought to −78° C.
  2. customgradually returning to room temperature
  3. waitAfter 2 hours 30 minutes
  4. customthe reaction mixture is precipitated from 2.5 liters of petroleum ether
  5. filtrationfiltered
  6. concentrationthe filtrate is concentrated to dryness
  7. customThe title product is purified by chromatography over silica gel (100% heptane)

出典と根拠

ORDレコード
ord-1998a41d3c444e92befe8253cdc01e54
出典データセット
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06638962B2

反応ノート

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