1,1-Dichloro-2,2-difluoroethene → Benzene, 1-(2,2-dichloro-3,3-difluorocyclobutyl)-4-methoxy-

HRID 258959

반응식

HRID 258959 반응식
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[CH2:8])=[CH:5][CH:4]=1.[Cl:11][C:12]([Cl:16])=[C:13]([F:15])[F:14].C(N(CC)CC)C>O>[Cl:11][C:12]1([Cl:16])[CH:7]([C:6]2[CH:9]=[CH:10][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[CH2:8][C:13]1([F:15])[F:14]

참가 물질

5

반응물 3

HCID 65921,1-Dichloro-2,2-difluoroetheneHCID 8471TriethylamineHCID 125074-Methoxystyrene

생성물 1

HCID 21425195Benzene, 1-(2,2-dichloro-3,3-difluorocyclobutyl)-4-methoxy-

시약·촉매·용매 1

HCID 962Water용매

실험 절차

p-Methoxystyrene (40.8 g., 0.30 mole), 1,1-dichloro-2,2-difluoroethylene (55.8 g., 0.42 mole), and triethylamine (3.0 ml., 0.02 mole) are heated in a sealed tube (25 × 615 mm) at 125°-130° C. for 16 hrs. The cooled mixture is then poured into water, the reaction product extracted with ether, and the extracts washed with water, dried (MgSO4), and evaporated to an oil. Distillation of the oil yields 69.0 g. (86%), b.p. 80°-85° C. (0.1 mm), of the desired intermediate sutiable for use in the next step. Part of the oil was chromatographed (alumina, cyclohexane), and redistilled, b.p. 81° C. (0.02 mm), nD27 1.5207.

후처리

  1. extractionthe reaction product extracted with ether
  2. washthe extracts washed with water
  3. dry with materialdried (MgSO4)
  4. customevaporated to an oil
  5. distillationDistillation of the oil
  6. customyields 69.0 g
  7. customPart of the oil was chromatographed (alumina, cyclohexane)
  8. distillationredistilled

출처 및 근거

ORD 기록
ord-38d988b8ebe3450c9217832735ceadc0
출처 데이터셋
uspto-grants-1977_07
특허 번호
US04035426

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