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

HRID 1655406
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HRID 1655406 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-hydroxybenzoic acid and 10 ml of dimethylformamide are mixed and heated. Carbon dioxide is evolved at 105°-130° C., and the reaction is allowed to come to an end at this temperature. 200 ml of toluene and then 80 ml of water are subsequently stirred in, the phases are separated, and the organic phase is dried and subsequently distilled. 34 g of the product of a boiling point of 87°-88° C. and a refractive index of nD20 : 1.5310 are obtained.

후처리

  1. temperatureheated
  2. customis evolved at 105°-130° C.
  3. customare separated
  4. customthe organic phase is dried
  5. distillationsubsequently distilled

출처 및 근거

ORD 기록
ord-88a63226dd7d477ebd29d403249a3ef4
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05250568

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