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

HRID 520433
Notes
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Reaction equation

HRID 520433 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6344Dichloromethane2×HCID 12041Ethyl pyruvateHCID 69808Allyltrimethylsilane

Product 1

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

Reagents, catalysts & solvents 1

HCID 24193Titanium TetrachlorideCatalyst

Procedure

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).

Workup

  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)

Sources & evidence

ORD record
ord-93eacaec2d724974a9c3e36db47660bb
Source dataset
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09326973B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes