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

HRID 1530059
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HRID 1530059 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 24648Sulfuryl chlorideHCID 10561837Ethyl 2-nitro-beta-oxobenzenepropanoate

생성물 1

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

시약·촉매·용매 1

HCID 3283Diethyl Ether
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-aab39fda02eb496a8bae7c5cb4448299
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09090601B2

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