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Water → Ethyl 2-chloro-3-(2-nitrophenyl)-3-oxopropanoate

HRID 2282222
ノート
印刷プレビュー

反応式

HRID 2282222 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10](=[O:17])[CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])([O-:3])=[O:2].S(Cl)([Cl:21])(=O)=O.O.CCOC(C)=O>C(OCC)C>[Cl:21][CH:11]([C:10]([C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[N+:1]([O-:3])=[O:2])=[O:17])[C:12]([O:14][CH2:15][CH3:16])=[O:13]
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 962WaterHCID 8857Ethyl AcetateHCID 24648Sulfuryl chlorideHCID 10561837Ethyl 2-nitro-beta-oxobenzenepropanoate

生成物 1

HCID 86649598Ethyl 2-chloro-3-(2-nitrophenyl)-3-oxopropanoate収率 75%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To a solution of ethyl 3-(2-nitrophenyl)-3-oxopropanoate (2.0 g, 8.4 mmol) in diethyl ether (50 mL), was added sulfuryl chloride (1.37 g, 10 mmol) at 0° C., and the mixture was stirred for 3 h at rt. To the reaction mixture were added water (200 mL) and EtOAc (100 mL), and the mixture was stirred for 30 min. The organic layer was washed with brine (10 mL) and dried over anhydrous magnesium sulfate. Insoluble materials were removed by filtration and the filtrate was concentrated under reduced pressure to give the title compound (1.7 g, 75%) as colorless oil.

後処理

  1. stirringthe mixture was stirred for 30 min
  2. washThe organic layer was washed with brine (10 mL)
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customInsoluble materials were removed by filtration
  5. concentrationthe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-1a7a59d42c174399ba42b10811930ef8
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09139589B2

反応ノート

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