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Oxalyl chloride → HCID 86585303、化合物

HRID 1168288
ノート
印刷プレビュー

反応式

HRID 1168288 の反応式
C(Cl)(=O)C(Cl)=O.[CH3:7][O:8][C@H:9]1[C@@H:13]2[O:14][C:15]([CH3:18])([CH3:17])[O:16][C@@H:12]2[C@@H:11]([C:19]([OH:21])=[O:20])[O:10]1.O[N:23]=[C:24]([NH2:27])[CH2:25][CH3:26].C(N(C(C)C)C(C)C)C>ClCCl.C(OCC)(=O)C>[CH3:7][O:8][C@H:9]1[C@@H:13]2[O:14][C:15]([CH3:18])([CH3:17])[O:16][C@@H:12]2[C@@H:11]([C:19]([O:21][N:23]=[C:24]([NH2:27])[CH2:25][CH3:26])=[O:20])[O:10]1
参加物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 65578Oxalyl chlorideHCID 81531DiisopropylethylamineHCID 4092053N-HydroxypropionimidamideHCID 10932896ST092333

生成物 1

HCID 86585303HCID 86585303、化合物収率 88.2%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒
HCID 8857
Ethyl Acetate
溶媒

実験手順

Oxalyl chloride (4 ml, 46 mmol) was added to a solution of (3aS,4S,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxylic acid (Justus Liebigs Ann. Chem., 1974, 11, 1856) (5 g, 23 mmol) in dichloromethane (100 ml). The solution was stirred at room temperature for two hours and then the solvent was evaporated under reduced pressure to yield a white solid. This was dissolved in ethyl acetate (80 ml) and N′-hydroxypropanimidamide (2.63 g, 30 mmol) was added followed by N-ethyldiisopropylamine (8.12 ml, 46 mmol). The reaction mixture was stirred at room temperature for 48 hours and then washed with saturated sodium hydrogencarbonate solution (50 ml) and brine (50 ml). The organic layer was separated, dried (anhydrous magnesium sulphate) and evaporated under reduced pressure to give the product as a dark yellow oil (5.85 g).

後処理

  1. customthe solvent was evaporated under reduced pressure
  2. customto yield a white solid
  3. stirringThe reaction mixture was stirred at room temperature for 48 hours
  4. washwashed with saturated sodium hydrogencarbonate solution (50 ml) and brine (50 ml)
  5. customThe organic layer was separated
  6. dry with materialdried (anhydrous magnesium sulphate)
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-e098c59da3e64362a248b7f904bf4b62
出典データセット
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06624158B2

反応ノート

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