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Water → Ethyl 4-chloro-2-(ethoxyimino)-3-oxobutanoate

HRID 543928
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HRID 543928 반응식
S(Cl)([Cl:4])(=O)=O.[CH2:6]([O:8][N:9]=[C:10]([C:16](=[O:18])[CH3:17])[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH3:7].O>C(O)(=O)C>[CH2:6]([O:8][N:9]=[C:10]([C:16](=[O:18])[CH2:17][Cl:4])[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 24648Sulfuryl chlorideHCID 54511140Ethyl 2-ethoxyimino-3-oxobutyrate

생성물 1

HCID 53877278Ethyl 4-chloro-2-(ethoxyimino)-3-oxobutanoate수율 93.1%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Sulfuryl chloride (35.2 g.) was added all at once to the stirred solution of ethyl 2-ethoxyimino-3-oxobutyrate (syn isomer, 48.9 g.) in acetic acid (49 ml.) at room temperature, and stirred at the same temperature for an hour. After adding the resultant solution into water (200 ml.), the solution was extracted with methylene chloride. The extract was washed with a saturated aqueous solution of sodium chloride, neutralized with an aqueous solution of sodium bicarbonate and washed with water. The solution was dried over magnesium sulfate and concentrated under reduced pressure to give ethyl 2-ethoxyimino-3-oxo-4-chlorobutyrate (syn isomer, 53.8 g.), pale yellow oil.

후처리

  1. extractionthe solution was extracted with methylene chloride
  2. washThe extract was washed with a saturated aqueous solution of sodium chloride
  3. washwashed with water
  4. dry with materialThe solution was dried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-6f6c7ee5ac0e436e8d2399952d7f565c
출처 데이터셋
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04447430

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