2,2,2-Trifluoro-1,1-ethanediol → Ethyl 2-methyl-4,4,4-trifluorocrotonate

HRID 1741924노트

반응식

HRID 1741924 반응식
[C:1]([CH2:6][CH:7]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:3][CH2:4][CH3:5])=[O:2].[CH:27](O)(O)[C:28]([F:31])([F:30])[F:29]>O1CCCC1>[CH3:7]/[C:6](=[CH:27]\[C:28]([F:31])([F:30])[F:29])/[C:1]([O:3][CH2:4][CH3:5])=[O:2]

참가 물질

4

반응물 2

HCID 679012,2,2-Trifluoro-1,1-ethanediolHCID 12607919Ethyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoate

생성물 1

HCID 5702867Ethyl 2-methyl-4,4,4-trifluorocrotonate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A suspension of (carbethoxyethylidene)triphenylphosphorane (400 g, 1.10 mole) in tetrahydrofuran (600 mL) was treated with aqueous fluoral hydrate (71.5% w/w, 180 g, 1.10 mole) over a period of 4 hours. During the addition the reaction temperature rose to 45° C. and all of the solid dissolved to give a clear brown solution. The mixture was allowed to stand for 15 hours and was then heated under reflux for 3.5 hours. The solution was distilled at 2,700 Pa until the temperature in the distillation flask reached 140° C., giving ethyl (E)-2-methyl-4,4,4-trifluorobut-2-enoate as a solution in tetrahydrofuran (Solution A, 0.75 L, containing a maximum of 201 g of alkene); NMR (270 MHz, CDCl3): 1.3 (t, 3H, J=7Hz), 2.1 (br, s, 3H), 4.3 (q, 2H, J=7Hz) and 6.7 (m, 1H), (plus signals due to tetrahydrofuran).

후처리

  1. additionDuring the addition the reaction temperature
  2. customrose to 45° C.
  3. dissolutionall of the solid dissolved
  4. customto give a clear brown solution
  5. temperaturewas then heated
  6. temperatureunder reflux for 3.5 hours
  7. distillationThe solution was distilled at 2,700 Pa until the temperature in the distillation flask
  8. customreached 140° C.

출처 및 근거

ORD 기록
ord-6c6222f8c4dc49cca11a7814ac577db6
출처 데이터셋
uspto-grants-1994_08
특허 번호
US05334765

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