18-Crown-6 → 2-Nitro 1-[di-(t-butyl)methoxy]propane

HRID 746185

反応式

HRID 746185 の反応式
[C:1]([CH:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[OH:6])([CH3:4])([CH3:3])[CH3:2].C([Li])(CC)C.C1OCCOCCOCCOCCOCCOC1.[N+:34]([C:37]([CH3:39])=[CH2:38])([O-:36])=[O:35]>C(#N)C.O1CCCC1>[N+:34]([CH:37]([CH3:39])[CH2:38][O:6][CH:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[C:1]([CH3:4])([CH3:3])[CH3:2])([O-:36])=[O:35]

参加物

7

反応物 4

HCID 2855718-Crown-6HCID 784862-Nitro-1-propeneHCID 1397902,2,4,4-Tetramethylpentan-3-olHCID 178418400CID 53628100

生成物 1

HCID 139072452-Nitro 1-[di-(t-butyl)methoxy]propane

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Di-t-butylmethanol is added to a dry flash under argon at 0° C. Dry tetrahydrofuran is added with a syringe. Sec-Butyl lithium (1.5M in Hexanes) is added quickly in one portion and the contents of the flask are stirred for one hour at room temperature. A 10 mM solution of 18-crown-6-ether in acetonitrile is added with a syringe and the flask cooled to 0° C. A tetrahydrofuran solution of 2-nitropropene is added with vigorous stirring over a 10 minute period. After completion of the reaction as judged by thin layer chromatography, it is quenched with saturated ammonium chloride and extracted with ethyl acetate. The organic layer is dried over MgSO4 and evaporated to yield 2-nitro 1-[di-(t-butyl)-methoxy]propane.

後処理

  1. temperaturethe flask cooled to 0° C
  2. stirringwith vigorous stirring over a 10 minute period
  3. customAfter completion of the reaction
  4. customis quenched with saturated ammonium chloride
  5. extractionextracted with ethyl acetate
  6. dry with materialThe organic layer is dried over MgSO4
  7. customevaporated

出典と根拠

ORDレコード
ord-77cd86b2f3c04eeaa2e3b9a757efb3c7
出典データセット
uspto-grants-1986_07
特許番号
US04603011

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