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Pentane → HCID 23114648、化合物

HRID 2080373
ノート
印刷プレビュー

反応式

HRID 2080373 の反応式
C([Li])(C)(C)C.CCCCC.[Si:11]([O:18][CH2:19][CH2:20][CH2:21][N:22]1[CH2:27][CH2:26][CH2:25][CH2:24][C:23]1=[O:28])([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12].[Br-:29].[Br-].[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC>CCCCCC.O.O1CCCC1>[Br:29][CH:24]1[CH2:25][CH2:26][CH2:27][N:22]([CH2:21][CH2:20][CH2:19][O:18][Si:11]([C:14]([CH3:16])([CH3:17])[CH3:15])([CH3:13])[CH3:12])[C:23]1=[O:28]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 8003PentaneHCID 231147471-(3-{[tert-Butyl(dimethyl)silyl]oxy}propyl)piperidin-2-oneHCID 23500184Tetra-n-butylammonium tribromideHCID 178418306HCID 178418306、化合物

生成物 1

HCID 23114648HCID 23114648、化合物収率 10.4%

試薬・触媒・溶媒 3

HCID 962
Water
溶媒
HCID 8028Tetrahydrofuran溶媒2 回
HCID 8058Hexane溶媒

反応条件

温度
-78 °C

実験手順

Under an argon atmosphere, t-butyl lithium (a 1.50M pentane solution, 1.40 ml, 2.10 mmol) was added dropwise to a tetrahydrofuran solution (5 ml) of 1-[3-(t-butyldimethylsilyloxy)propyl]piperidin-2-one (542 mg, 2.00 mmol) at −78° C. The reaction mixture was stirred at −78° C. for 15 minutes. After a tetrahydrofuran solution (5 ml) of tetrabutylammonium tribromide (1.16 g, 2.40 mmol) was added to the reaction mixture, the temperature of the resulting mixture was gradually raised to −40° C. under stirring. Water was added to the reaction mixture at −40° C. and then, the temperature of the mixture was raised to room temperature. The reaction mixture was extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate and concentrated. The residue thus obtained was subjected to flash silica gel column chromatography. The fraction obtained from the hexane:ethyl acetate=2:3 eluate was concentrated to give the title compound (72.8 mg, 0.208 mmol, 10%) as a colorless oil.

後処理

  1. temperaturethe temperature of the resulting mixture was gradually raised to −40° C.
  2. stirringunder stirring
  3. temperaturethe temperature of the mixture was raised to room temperature
  4. extractionThe reaction mixture was extracted with ethyl acetate
  5. washThe extract was washed with water and brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated
  8. customThe residue thus obtained
  9. concentrationethyl acetate=2:3 eluate was concentrated

出典と根拠

ORDレコード
ord-85234d62d942484c9123e0fcb34ddba2
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07932271B2

反応ノート

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