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Chlorotrimethylsilane → 2-Butyrylaminobutyric acid

HRID 11254
ノート
印刷プレビュー

反応式

HRID 11254 の反応式
[NH2:1][CH:2]([CH2:6][CH3:7])[C:3]([OH:5])=[O:4].C(N(CC)CC)C.C[Si](Cl)(C)C.[C:20](Cl)(=[O:24])[CH2:21][CH2:22][CH3:23].[OH-].[Na+]>ClCCl.O>[C:20]([NH:1][CH:2]([CH2:6][CH3:7])[C:3]([OH:5])=[O:4])(=[O:24])[CH2:21][CH2:22][CH3:23]
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 5

HCID 6397ChlorotrimethylsilaneHCID 6657Alpha-Aminobutyric AcidHCID 8471TriethylamineHCID 8855Butyryl chlorideHCID 14798Sodium Hydroxide

生成物 1

HCID 124088662-Butyrylaminobutyric acid

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

25.78 g of 2-aminobutyric acid (250 mmol) and 55.66 g (550 mmol) of triethylamine are dissolved in 250 ml of dichloromethane, and the solution is cooled to 0° C. 59.75 g (550 mmol) of trimethylsilyl chloride are added dropwise, and the solution is stirred at room temperature for 1 hour and at 40° C. for one hour. After cooling to −10° C., 26.64 g (250 mmol) of butyryl chloride are added dropwise, and the resulting mixture is stirred at −10° C. for 2 hours and at room temperature for one hour. With ice-cooling, 125 ml of water are added dropwise, and the reaction mixture is stirred at room temperature for 15 minutes. Aqueous sodium hydroxide solution is added to the organic phase, and the organic solvent is removed under reduced pressure. The residue is acidified and the precipitated solid is triturated once with water and twice with petroleum ether and dried under reduced pressure at 45° C. 29.1 g (67%) of a colorless solid.

後処理

  1. temperatureAfter cooling to −10° C.
  2. stirringthe resulting mixture is stirred at −10° C. for 2 hours and at room temperature for one hour
  3. temperatureWith ice-cooling
  4. stirringthe reaction mixture is stirred at room temperature for 15 minutes
  5. customthe organic solvent is removed under reduced pressure
  6. customthe precipitated solid is triturated once with water and twice with petroleum ether
  7. customdried under reduced pressure at 45° C

出典と根拠

ORDレコード
ord-46b5a06419784ab4aa0ab701d258a09a
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07098207B2

反応ノート

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