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Dichloromethane → ethyl 2-hydroxy-2-methylpent-4-enoate

HRID 520433
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HRID 520433 반응식
[O:1]=[C:2]([CH3:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4].[CH2:9]([Si](C)(C)C)[CH:10]=C.Cl[CH2:17]Cl>[Ti](Cl)(Cl)(Cl)Cl>[OH:1][C:2]([CH3:17])([CH2:8][CH:9]=[CH2:10])[C:3]([O:5][CH2:6][CH3:7])=[O:4]
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참가 물질

5

반응물 3

HCID 6344Dichloromethane2회HCID 12041Ethyl pyruvateHCID 69808Allyltrimethylsilane

생성물 1

HCID 10909832ethyl 2-hydroxy-2-methylpent-4-enoate수율 58.7%

시약·촉매·용매 1

HCID 24193Titanium Tetrachloride촉매

실험 절차

Ethyl 2-oxopropanoate (1 g, 8.61 mmol) was taken in to DCM (5M) and cooled to −78 C. To this titanium tetrachloride (8.61 mL, 8.61 mmol) in dichloromethane (5 mL) was added and stirred the reaction mixture for 30 min at this temperature. To this reaction mixture allyltrimethylsilane (1.279 g, 11.20 mmol) was added drop wise at −78° C. and stirring was continued for 2 h. Then it was brought to 0° C. and quenched with saturated aq. sodium bicarbonate solution and stirred for 15 min, and filtered through celite bed and filtrate was evaporated under reduced pressure to afford colorless oil. The residue was purified by flash chromatography (silica, 230-400, 10% EtoAc/Pet ether) to obtain ethyl 2-hydroxy-2-methylpent-4-enoate B-37a (0.8 g, 5.06 mmol, 58.7% yield) as yellow liquid. 1H NMR (CDCl3, δ=7.26 ppm, 400 MHz): δ 5.84-5.72 (m, 1H), 5.15-5.09 (m, 2H), 4.29-4.19 (m, 2H), 2.56-2.37 (m, 2H), 1.43 (s, 3H), 1.31 (t, J=9.6 Hz, 3H).

후처리

  1. temperaturecooled to −78 C
  2. stirringstirring
  3. waitwas continued for 2 h
  4. customwas brought to 0° C.
  5. customquenched with saturated aq. sodium bicarbonate solution
  6. stirringstirred for 15 min
  7. filtrationfiltered through celite bed and filtrate
  8. customwas evaporated under reduced pressure
  9. customto afford colorless oil
  10. customThe residue was purified by flash chromatography (silica, 230-400, 10% EtoAc/Pet ether)

출처 및 근거

ORD 기록
ord-93eacaec2d724974a9c3e36db47660bb
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09326973B2

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