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Ethyl chloroacetate → HCID 55288043、化合物

HRID 249846
ノート
印刷プレビュー

反応式

HRID 249846 の反応式
[H-].[Na+].[NH2:3][C@@H:4]([CH:7]([CH3:9])[CH3:8])[CH2:5][OH:6].Cl[CH2:11][C:12](OCC)=[O:13].[Cl-].[NH4+]>C1(C)C=CC=CC=1>[CH:7]([C@@H:4]1[NH:3][C:12](=[O:13])[CH2:11][O:6][CH2:5]1)([CH3:9])[CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 7751Ethyl chloroacetateHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 640993L-Valinol

生成物 1

HCID 55288043HCID 55288043、化合物収率 67%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒3 回

実験手順

To an ice cold, stirred suspension of sodium hydride (60% in oil, 1.3 g, 34.0 mmol) in toluene (45 mL) was added dropwise a solution of (S)-2-amino-3-methylbutan-1-ol (1.5 g, 15.0 mmol) in toluene (30 mL). After the addition was complete, the reaction mixture was warmed to room temperature and a solution of ethyl chloroacetate (2.0 g, 16.0 mmol) in toluene (8 mL) was added in a dropwise manner. The resulting mixture was then stirred at reflux for 20 h, cooled to room temperature, and solid ammonium chloride (1.8 g, 34.0 mmol) added to the reaction. The mixture was stirred for 20 min and then concentrated under reduced pressure. The crude material was purified by column chromatography (silica gel, 95:5 CH2Cl2/CH3OH) to give (S)-5-isopropylmorpholin-3-one (1.4 g, 67%) as a light yellow solid. 1H NMR and MS consistent.

後処理

  1. additionAfter the addition
  2. temperatureat reflux for 20 h
  3. temperaturecooled to room temperature
  4. stirringThe mixture was stirred for 20 min
  5. concentrationconcentrated under reduced pressure
  6. customThe crude material was purified by column chromatography (silica gel, 95:5 CH2Cl2/CH3OH)

出典と根拠

ORDレコード
ord-8d81f7b334034ee8a91aa36b4c02a200
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07863271B2

反応ノート

読み込み中…

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