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Ethylene Glycol → Ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate

HRID 463381
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HRID 463381 반응식
[CH3:1][O:2][N:3]=[C:4]([C:10](=[O:13])[CH2:11][Cl:12])[C:5]([O:7][CH2:8][CH3:9])=[O:6].[CH2:14](O)[CH2:15][OH:16].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH3:1][O:2][N:3]=[C:4]([C:10]1([O:16][CH2:15][CH2:14][O:13]1)[CH2:11][Cl:12])[C:5]([O:7][CH2:8][CH3:9])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 174Ethylene GlycolHCID 6101p-Toluenesulfonic acidHCID 3017525Ethyl 4-chloro-2-(methoxyimino)-3-oxobutanoate

생성물 1

HCID 54025463Ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate수율 49.1%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of ethyl 2-methoxyimino-3-oxo-4-chlorobutyrate (syn isomer, 41 g), ethylene glycol (24.6 g), p-toluenesulfonic acid (2.0 g) and toluene (250 ml) was heated for 20 hours under reflux while removing water. The reaction mixture was cooled to ambient temperature, washed with a saturated aqueous solution of sodium bicarbonate, a saturated aqueous solution of sodium chloride in turn, dried over magnesium sulfate and then the solvents were removed. The residue was distilled under reduced pressure to give ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate (syn isomer, 24.4 g), bp 103°-110° C./2 mmHg.

후처리

  1. temperaturewas heated for 20 hours
  2. temperatureunder reflux
  3. customwhile removing water
  4. washwashed with a saturated aqueous solution of sodium bicarbonate
  5. dry with materiala saturated aqueous solution of sodium chloride in turn, dried over magnesium sulfate
  6. customthe solvents were removed
  7. distillationThe residue was distilled under reduced pressure

출처 및 근거

ORD 기록
ord-916d4646fa0549f4be54316a8e4b9972
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04518774

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