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Carbon Dioxide → 2,6-Dichloro-3,5-difluorophenol

HRID 345868
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HRID 345868 반응식
[Cl:1][C:2]1[C:3]([F:14])=[C:4]([C:8]([F:13])=[C:9]([Cl:12])[C:10]=1[OH:11])C(O)=O.CN(C)C=O.C(=O)=O.C1(C)C=CC=CC=1>O>[Cl:1][C:2]1[C:3]([F:14])=[CH:4][C:8]([F:13])=[C:9]([Cl:12])[C:10]=1[OH:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 280Carbon DioxideHCID 1140TolueneHCID 6228DimethylformamideHCID 14404998HCID 14404998, 화합물

생성물 1

HCID 27825072,6-Dichloro-3,5-difluorophenol수율 83%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

50 g of 3,5-dichloro-2,6-difluoro-4-hydroxy-benzoic acid and 10 ml of dimethylformamide are mixed and heated. At 105°-130° C., carbon dioxide evolves, and the reaction is allowed to proceed to completion at this temperature. 200 ml of toluene and 80 ml of water are then added in succession, the phases are separated, and the organic phase is dried and then distilled. 34 g of the product of a boiling point of 87°-88° C. and refractive index of nD20 : 1.5310 are obtained.

후처리

  1. temperatureheated
  2. customAt 105°-130° C.
  3. customthe phases are separated
  4. customthe organic phase is dried
  5. distillationdistilled

출처 및 근거

ORD 기록
ord-34b8b9b0f5eb429e95851bddf2ba735a
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05059623

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