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Ammonium Chloride → HCID 69559116、化合物

HRID 2213024
ノート
印刷プレビュー

反応式

HRID 2213024 の反応式
[N:1]1([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:6][CH2:5][CH:4]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2]1.C[Si](C)(C)[N-][Si](C)(C)C.[K+].Br[CH2:30][C:31]([CH3:33])=[CH2:32].[Cl-].[NH4+]>O1CCCC1.O>[CH3:32][C:31](=[CH2:30])[CH2:33][C:4]1([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2][N:1]([C:12]([O:14][C:15]([CH3:17])([CH3:16])[CH3:18])=[O:13])[CH2:6][CH2:5]1
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

7

反応物 4

HCID 25517Ammonium ChlorideHCID 3577853-Bromo-2-methyl-1-propeneHCID 27588121-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 3251421Potassium bis(trimethylsilyl)amide

生成物 1

HCID 69559116HCID 69559116、化合物収率 99.4%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

A solution of 1-(1,1-dimethylethyl) 4-ethyl 1,4-piperidinedicarboxylate (12.85 g, 50 mmol) in tetrahydrofuran (50 mL) was added slowly to a stirred, cooled (−78° C.) solution of potassium hexamethyldisilazide (14.96 g, 75 mmol) in tetrahydrofuran (75 mL), maintaining the internal temperature below −65° C. The mixture was stirred at −78° C. for 30 minutes, then 3-bromo-2-methylpropene (7.56 mL, 10.12 g, 75 mmol) was added dropwise over 5 minutes. The mixture was stirred at −78° C. for 1 hour, then saturated aqueous ammonium chloride (200 mL) was added and the mixture was warmed to room temperature. Water (100 mL) was added and the mixture was extracted with ethyl acetate (3×200 mL). The combined organic fractions were washed with aqueous citric acid (10%, 3×200 mL), saturated aqueous sodium hydrogen carbonate (200 mL) and brine (200 mL), dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound as a pale yellow oil (15.48 g, 99%). m/z (ES+) 256 (M+1-C4H8).

後処理

  1. temperaturemaintaining the internal temperature below −65° C
  2. stirringThe mixture was stirred at −78° C. for 1 hour
  3. temperaturethe mixture was warmed to room temperature
  4. extractionthe mixture was extracted with ethyl acetate (3×200 mL)
  5. washThe combined organic fractions were washed with aqueous citric acid (10%, 3×200 mL), saturated aqueous sodium hydrogen carbonate (200 mL) and brine (200 mL)
  6. dry with materialdried (MgSO4)
  7. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-565af6031dae45718f9e802271fd124d
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07105507B2

反応ノート

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