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1,3-Dioxolane, 2-(4-fluoro-3-phenoxyphenyl)- → 4-Fluoro-3-phenoxybenzaldehyde

HRID 231320
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HRID 231320 반응식
C1O[CH:4]([C:5]2[CH:10]=[CH:9][C:8]([F:11])=[C:7]([O:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH:6]=2)[O:3]C1>C(O)C.O.Cl>[F:11][C:8]1[CH:9]=[CH:10][C:5]([CH:4]=[O:3])=[CH:6][C:7]=1[O:12][C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1
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참가 물질

5

반응물 1

HCID 119706461,3-Dioxolane, 2-(4-fluoro-3-phenoxyphenyl)-

생성물 1

HCID 1100684-Fluoro-3-phenoxybenzaldehyde수율 91%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 702Ethanol용매HCID 962Water용매

실험 절차

A solution of 26 g (0.1 mol) of 4-fluoro-3-phenoxy-benzaldehyde ethyleneacetal in 60 ml of ethanol, 20 ml of water and 1 ml of concentrated hydrochloric acid was stored at room temperature for 3 hours. The ethanol was then distilled off in vacuo, and 100 ml of toluene were added to the residue. The water was separated off and the organic phase was washed twice with 50 ml of water each time, dried over sodium sulphate and evaporated in vacuo. The residue was distilled in vacuo. 19.6 g (91% of theory) of 4-fluoro-3-phenoxy-benzaldehyde were obtained in this manner in the form of a colorless oil with a boiling point of 102°-104° C./0.1 mm Hg.

후처리

  1. distillationThe ethanol was then distilled off in vacuo, and 100 ml of toluene
  2. additionwere added to the residue
  3. customThe water was separated off
  4. washthe organic phase was washed twice with 50 ml of water each time
  5. dry with materialdried over sodium sulphate
  6. customevaporated in vacuo
  7. distillationThe residue was distilled in vacuo

출처 및 근거

ORD 기록
ord-af38d85afc5a4721a04111f7faff4646
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04845249

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