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Allyltrimethylsilane → (2S,5R)-5-Allyl-1-methyl-pyrrolidine-2-carboxylic acid phenethyl-amide

HRID 1668422
ノート
印刷プレビュー

反応式

HRID 1668422 の反応式
[CH2:1]([NH:9][C:10]([C@@H:12]1[CH2:16][CH2:15][CH:14](OC)[N:13]1[CH3:19])=[O:11])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:20]([Si](C)(C)C)[CH:21]=[CH2:22]>[Ti](Cl)(Cl)(Cl)Cl.ClCCl>[CH2:1]([NH:9][C:10]([C@@H:12]1[CH2:16][CH2:15][C@H:14]([CH2:22][CH:21]=[CH2:20])[N:13]1[CH3:19])=[O:11])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 69808AllyltrimethylsilaneHCID 66995375(S)-5-Methoxy-1-methyl-pyrrolidine-2-carboxylic acid phenethyl-amide

生成物 1

HCID 68811256(2S,5R)-5-Allyl-1-methyl-pyrrolidine-2-carboxylic acid phenethyl-amide

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒HCID 6344Dichloromethane溶媒

実験手順

A dichloromethane (20 mL) solution of 11C methylaminal (7.7 g, 20 mmol) is chilled to −78° C. After 20 minutes, allyltrimethylsilane (6.5 mL, 40 mmol) is added. After 10 more minutes 1 M titanium(IV) chloride (24 mL, 24 mmol) is added slowly by syringe. The reaction is complete after 1 hour. The resulting material is carefully quenched (frothing) with saturated bicarb and extracted with dichlormethane, then washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The product is isolated by flash chromatography (SiO2), and it crystallizes upon standing. LCMS characterization ES+393.1 (m+1).

後処理

  1. waitThe reaction is complete after 1 hour
  2. customThe resulting material is carefully quenched (frothing) with saturated bicarb
  3. extractionextracted with dichlormethane
  4. washwashed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe product is isolated by flash chromatography (SiO2), and it
  9. customcrystallizes

出典と根拠

ORDレコード
ord-8c832a7320bd4faa8bfe16efefa5eb7d
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07989441B2

反応ノート

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