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Bromine → Ethyl 3-bromo-2-oxocyclohexanecarboxylate

HRID 1394102
ノート
印刷プレビュー

反応式

HRID 1394102 の反応式
[O:1]=[C:2]1[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]1[C:8]([O:10][CH2:11][CH3:12])=[O:9].[Br:13]Br>C(Cl)(Cl)Cl>[Br:13][CH:7]1[CH2:6][CH2:5][CH2:4][CH:3]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[C:2]1=[O:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24408BromineHCID 95543Ethyl 2-oxocyclohexanecarboxylate

生成物 1

HCID 121765Ethyl 3-bromo-2-oxocyclohexanecarboxylate

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To a solution of ethyl 2-oxocyclohexanecarboxylate (50 g, 0.29 mol) in CHCl3 (150 mL) there was slowly added bromine (47 g, 0.29 mol) at 0° C. under a blanket of nitrogen as inert gas dropwise over a period of 45 minutes and the resultant mixture was stirred for a period of 6 hours at 0° C. and then for 16 hours at room temperature. Air was then passed into the reaction solution over a period of 2 hours. The organic phase was washed with aqueous saturated NaHCO3 solution (2×15 mL) and aqueous saturated NaCl solution (3×20 mL). Following drying of the organic phase over Na2SO4 and filtration, the solvent was removed. The product ethyl 3-bromo-2-oxocyclohexanecarboxylate was obtained in a yield of 72.6 g (corresponding to 99% of theory).

後処理

  1. customat 0° C.
  2. customof 45 minutes
  3. waitAir was then passed into the reaction solution over a period of 2 hours
  4. washThe organic phase was washed with aqueous saturated NaHCO3 solution (2×15 mL) and aqueous saturated NaCl solution (3×20 mL)
  5. dry with materialFollowing drying of the organic phase over Na2SO4 and filtration
  6. customthe solvent was removed

出典と根拠

ORDレコード
ord-0ef8df6ab1f342108347979d946b8734
出典データセット
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07348347B2

反応ノート

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