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Ethylene Glycol → 2-(2-Bromoethyl)-2-methyl-1,3-dioxolane

HRID 1106293
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인쇄 미리보기

반응식

HRID 1106293 반응식
[Br:1][CH2:2][CH2:3][C:4](=[O:6])[CH3:5].[CH2:7](O)[CH2:8][OH:9].C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)([O-])[O-].[K+].[K+]>C(OCC)(=O)C.O.C1(C)C=CC=CC=1>[CH2:8]1[O:9][C:4]([CH2:3][CH2:2][Br:1])([CH3:5])[O:6][CH2:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 174Ethylene GlycolHCID 6101p-Toluenesulfonic acidHCID 11430Potassium CarbonateHCID 124527344-Bromobutan-2-one

생성물 1

HCID 118056192-(2-Bromoethyl)-2-methyl-1,3-dioxolane

시약·촉매·용매 3

HCID 962Water용매HCID 1140Toluene용매

실험 절차

A mixture of 75 g of 4-bromo-2-butanone, 40 g of ethylene glycol, 250 mg of p-toluenesulfonic acid acid and 500 ml of toluene is refluxed for about 4-6 hours under a Dean-Stark water trap. The mixture is cooled, poured into ethyl acetate and dilute potassium carbonate solution. The organic layer is separated, washed with water, dried over sodium sulfate, stripped of solvent and the residue is distilled under reduced pressure to give the title product.

후처리

  1. temperatureThe mixture is cooled
  2. customThe organic layer is separated
  3. washwashed with water
  4. dry with materialdried over sodium sulfate
  5. distillationthe residue is distilled under reduced pressure

출처 및 근거

ORD 기록
ord-5579699143fc4414b844206821a3455e
출처 데이터셋
uspto-grants-1982_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04312994

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 8857
Ethyl Acetate
용매