Glycol monoethyl ether acetate → Pentachlorophenyl perfluoroethoxymethyl ketone

HRID 279689

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HRID 279689 반응식
Cl[C:2]1[C:7]([Cl:8])=[C:6]([Cl:9])[C:5]([Cl:10])=[C:4]([Cl:11])[C:3]=1[Cl:12].C([Li])CCC.[F:18][C:19]([F:31])([O:23][C:24]([F:30])([F:29])[C:25]([F:28])([F:27])[F:26])[C:20](F)=[O:21].C(OCCOCC)(=O)C>C(OCC)C>[F:18][C:19]([C:20]([C:2]1[C:3]([Cl:12])=[C:4]([Cl:11])[C:5]([Cl:10])=[C:6]([Cl:9])[C:7]=1[Cl:8])=[O:21])([F:31])[O:23][C:24]([F:29])([F:30])[C:25]([F:26])([F:28])[F:27]

참가 물질

6

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온도
-40 °C

실험 절차

Hexachlorobenzene (35 g) was slurried in 160 ml of anhydrous ethyl ether at −40° C. A 2.5 M hexanes solution of n-butyllithium (54.1 mL) was added, and the reaction was stirred for 30 minutes at −40° C. Perfluoro-2-ethoxyacetylfluoride (40 g, 72% pure, prepared from 2-ethoxyethyl acetate by the method described in Example 1 of U.S. Pat. No. 5,326,919, incorporated herein by reference) was added to the −40° C. reaction mixture which was then allowed to warm slowly to room temperature. The reaction mixture was quenched with 200 mL of cold 5% aqueous HCl. The aqueous mixture was extracted with ethyl ether and the extracts were dried over MgSO4 and rotary evaporated to give pentachlorophenyl perfluoroethoxymethyl ketone (49% crude yield). Vacuum distillation (105-109° C., 240 Pa) using a 15 cm Vigreux column gave 19.7 g of a colorless liquid which slowly crystallized on standing.

후처리

  1. addition5,326,919, incorporated herein by reference) was added to the −40° C. reaction mixture which
  2. temperatureto warm slowly to room temperature
  3. customThe reaction mixture was quenched with 200 mL of cold 5% aqueous HCl
  4. extractionThe aqueous mixture was extracted with ethyl ether
  5. dry with materialthe extracts were dried over MgSO4
  6. customrotary evaporated

출처 및 근거

ORD 기록
ord-4a6918a974974769baef6bfa191c1207
출처 데이터셋
uspto-grants-2002_03
특허 번호
US06362379B1

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