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

HRID 374301
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HRID 374301 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-difluorophenol

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 the mixture is heated. Carbon dioxide is evolved at 105°-130° C., and the mixture is allowed to react at this temperature until the reaction is complete. After this, 200 ml of toluene and then 80 ml of water are stirred in, the phases are separated, and the organic phase is dried and then distilled. This gives 34 g of the product having a boiling point of 87°-88° C. and a refractive index of [n]D20 : 1.5310.

후처리

  1. temperaturethe mixture is heated
  2. customis evolved at 105°-130° C.
  3. customto react at this temperature until the reaction
  4. customare separated
  5. customthe organic phase is dried
  6. distillationdistilled

출처 및 근거

ORD 기록
ord-d60ebe012c544bc693d0978ccf5ab60d
출처 데이터셋
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05166392

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