Ethylene Glycol → 2-Phenyl-2-(2-thienyl)-1,3-dioxolane

HRID 1262946노트

반응식

HRID 1262946 반응식
[C:1]([C:9]1[S:10][CH:11]=[CH:12][CH:13]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.[CH2:21](O)[CH2:22][OH:23]>C1(C)C=CC(S(O)(=O)=O)=CC=1>[C:2]1([C:1]2([C:9]3[S:10][CH:11]=[CH:12][CH:13]=3)[O:23][CH2:22][CH2:21][O:8]2)[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

5

반응물 3

HCID 174Ethylene Glycol2회HCID 1140TolueneHCID 672622-Benzoylthiophene

생성물 1

HCID 129626732-Phenyl-2-(2-thienyl)-1,3-dioxolane

시약·촉매·용매 1

HCID 6101p-Toluenesulfonic acid촉매

실험 절차

2-Benzoylthiophene (19 g., 0.1 mole), ethylene glycol (11 ml., 0.2 mole), toluene (150 ml.) and p-toluenesulfonic acid (about 0.2 g.) were combined and refluxed for 6 hours. By-product water was collected in a Dean-Stark trap. Tlc (1:8 ethyl acetate:hexane) indicated reaction to be about 40% complete. More ethylene glycol (30 ml.) was added and reflux continued for 35 hours. Reaction was still incomplete. The reaction mixture was diluted with 200 ml. of ether, washed twice with 150 ml. portions of water and concentrated to dryness. The residue was chromatographed on about 500 ml. of silica gel, with 1:8 ethyl acetate:hexane as eluant, monitored by tlc. Faster moving, product containing fractions were combined and evaporated to yield 2-phenyl-2-(2-thienyl)-1,3-dioxolane [8 g., oil, Rf 0.6 (1:8 ethyl acetate:hexane)].

후처리

  1. temperaturerefluxed for 6 hours
  2. customBy-product water was collected in a Dean-Stark trap
  3. customreaction
  4. temperaturereflux
  5. customReaction
  6. additionThe reaction mixture was diluted with 200 ml
  7. washof ether, washed twice with 150 ml
  8. concentrationportions of water and concentrated to dryness
  9. customThe residue was chromatographed on about 500 ml
  10. additionproduct containing fractions
  11. customevaporated

출처 및 근거

ORD 기록
ord-436da4dd285d4a1aae632fa3b7699d33
출처 데이터셋
uspto-grants-1984_06
특허 번호
US04454320

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