Acetone → 4-[(Allyloxy)methyl]-2,2-dimethyl-1,3-dioxolane

HRID 1165115

반응식

HRID 1165115 반응식
[CH3:1][C:2]([CH3:4])=O.[CH2:5]([O:8][CH2:9][CH:10]([OH:13])[CH2:11][OH:12])[CH:6]=[CH2:7].S(=O)(=O)(O)O>C1(C)C=CC=CC=1>[CH2:5]([O:8][CH2:9][CH:10]1[CH2:11][O:12][C:2]([CH3:4])([CH3:1])[O:13]1)[CH:6]=[CH2:7]

참가 물질

5

반응물 3

HCID 180AcetoneHCID 1118Sulfuric AcidHCID 78950Glyceryl Allyl Ether

생성물 1

HCID 27801544-[(Allyloxy)methyl]-2,2-dimethyl-1,3-dioxolane

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

The 4-allyloxymethyl-2,2-dimethyl-1,3-dioxolane was prepared by mixing acetone, 225 parts, 3-allyloxy-1,2-propanediol, 195 parts and toluene, 480 parts in a flask fitted with a magnetic stirring bar and a water trap mounted with a reflux condenser. Concentrated sulfuric acid, 4 parts, was added to the flask and the mixture was heated to reflux. The first 170 parts of distillate were removed via the water trap, after which reflux was conducted and water was collected in the water trap. After 13 hours the reaction mixture was cooled, neutralized with aqueous sodium bicarbonate, distilled to remove water and toluene and then distilled under vacuum to give 161 parts of 4-allyloxymethyl-2,2-dimethyl-1,3-dioxolane having a boiling point of 57° to 58° at 4.5 Torr.

후처리

  1. customThe 4-allyloxymethyl-2,2-dimethyl-1,3-dioxolane was prepared
  2. customfitted with a magnetic stirring bar and a water trap
  3. custommounted with a reflux condenser
  4. temperaturethe mixture was heated to reflux
  5. customThe first 170 parts of distillate were removed via the water trap
  6. temperatureafter which reflux
  7. customwater was collected in the water trap
  8. temperatureAfter 13 hours the reaction mixture was cooled
  9. distillationdistilled
  10. customto remove water and toluene
  11. distillationdistilled under vacuum

출처 및 근거

ORD 기록
ord-0f33f28672da42469efd880561463591
출처 데이터셋
uspto-grants-1990_03
특허 번호
US04908228

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