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Chlorotrimethylsilane → HCID 19974944、化合物

HRID 1451518
ノート
印刷プレビュー

反応式

HRID 1451518 の反応式
[CH3:1][Li].C[Si](Cl)(C)C.[Br:8][C:9]1[CH:34]=[CH:33][C:12]([CH2:13][N:14]2[C:22]3[C:17](=[CH:18][C:19]([O:23][CH3:24])=[CH:20][CH:21]=3)[C:16]([CH:25]=[CH:26][C:27]([O:29][CH2:30][CH3:31])=[O:28])=[C:15]2[CH3:32])=[CH:11][CH:10]=1.[NH4+].[Cl-]>CCOCC.C1COCC1>[Br:8][C:9]1[CH:34]=[CH:33][C:12]([CH2:13][N:14]2[C:22]3[C:17](=[CH:18][C:19]([O:23][CH3:24])=[CH:20][CH:21]=3)[C:16]([CH:25]([CH3:1])[CH2:26][C:27]([O:29][CH2:30][CH3:31])=[O:28])=[C:15]2[CH3:32])=[CH:11][CH:10]=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 6397ChlorotrimethylsilaneHCID 25517Ammonium ChlorideHCID 54298386HCID 54298386、化合物HCID 178418348HCID 178418348、化合物

生成物 1

HCID 19974944HCID 19974944、化合物収率 73.1%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
-78 °C

実験手順

To a 0° C. suspension of cuprous iodide (12.7 g, 67.0 mmol) in 150 mL ether was added CH3Li (1.4M in ether, 96 mL, 134 mmol). The solution was cooled to -78° C. and treated with TMSCl (8.5 mL, 67 mmol) and a solution of the unsaturated ester from Step 3 (6.79 g, 15.8 mmol) in 30 mL of THF. The yellow suspension was allowed to warm to room temperature and was stirred 2.5 h. The reaction mixture was poured into saturated NH4Cl and extracted with EtOAc. The organic extracts were washed with water and brine and dried over Na2SO4. Purification by flash chromatography (20% ethyl acetate/hexanes) provided 5.13 g of the title product as a crystaline solid.

後処理

  1. temperatureto warm to room temperature
  2. extractionextracted with EtOAc
  3. washThe organic extracts were washed with water and brine
  4. dry with materialdried over Na2SO4
  5. customPurification by flash chromatography (20% ethyl acetate/hexanes)

出典と根拠

ORDレコード
ord-cbe3cc555118478e8ebbb18f459c0fba
出典データセット
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05604253

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート