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Diethyl Malonate → HCID 67099102、化合物

HRID 1868628
ノート
印刷プレビュー

反応式

HRID 1868628 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:13])([CH3:12])[C:9]([OH:11])=O)=[CH:4][CH:3]=1.C(Cl)(=O)C(Cl)=O.[C:20]([O:28][CH2:29][CH3:30])(=[O:27])[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23].[Mg+2].[Cl-].[Cl-].C([O-])(=O)CC([O-])=O>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([CH3:13])([CH3:12])[C:9]([CH:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[C:20]([O:28][CH2:29][CH3:30])=[O:27])=[O:11])=[CH:6][CH:7]=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 5

HCID 7761Diethyl MalonateHCID 9084Malonate IonHCID 65578Oxalyl chlorideHCID 804062-(4-Chlorophenyl)-2-methylpropionic acidHCID 5360315Magnesium Chloride

生成物 1

HCID 67099102HCID 67099102、化合物

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

A solution of 2-(4-chlorophenyl)-2-methylpropionic acid (1.99 g, 10.0 mmol, 1.0 eq.) in IPAc (10 mL) was treated with DMF (0.02 mL) and oxalyl chloride (0.92 mL, 10.5 mmol). The resulting solution was stirred at room temperature for 2 hours. In a separate vessel, was charged diethyl malonate (1.91 mL, 12.5 mmol), IPAc (14 mL), and MgCl2 (11.9 g, 12.5 mmol). The resulting malonate slurry was stirred at room temperature for 30 minutes and subsequently treated with TEA (4.7 mL, 33.5 mmol). The resulting suspension was aged at room temperature for 2 hours, cooled to 5° C. and treated with the above acyl chloride solution. The resulting mixture was warmed to ambient temperature and aged for 1 hour. The slurry was quenched with a 5N HCl solution (10 mL) and the phases were split. The organic phase was washed with saturated NaHCO3 solution (2×10 mL) and water (1×10 mL). The organic phase was dried (MgSO4) and concentrated in vacuo to afford an orange oil. MS m/e=341.2 (M+H)+.

後処理

  1. waitThe resulting suspension was aged at room temperature for 2 hours
  2. temperaturecooled to 5° C.
  3. temperatureThe resulting mixture was warmed to ambient temperature and aged for 1 hour
  4. customThe slurry was quenched with a 5N HCl solution (10 mL)
  5. customthe phases were split
  6. washThe organic phase was washed with saturated NaHCO3 solution (2×10 mL) and water (1×10 mL)
  7. dry with materialThe organic phase was dried (MgSO4)
  8. concentrationconcentrated in vacuo
  9. customto afford an orange oil

出典と根拠

ORDレコード
ord-49de6bd3743342abbef273385eb46931
出典データセット
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07635715B2

反応ノート

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