Réaction #1755470

ord-602fcd423d8c431b838d56a3d1c67203

Équation de réaction

C#CCC1CCC(C(=O)O)CC1
88
C#CCC1CCC(C(=O)O)CC1
4-prop-2-ynyl-cyclohexanecarboxylic acid
ClCCl
CH2Cl2
CO
MeOH
C[Si](C)(C)C=[N+]=[N-]
TMS Diazomethane
C#CCC1CCC(C(=O)OC)CC1
89
Rendement 80.0%
C#CCC1CCC(C(=O)OC)CC1
Methyl 4-prop-2-ynylcyclohexanecarboxylate
Rendement 80.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGAfter stirring
  2. 2
    ConcentrationThe reaction was concentrated in vacuo to an oil which
  3. 3
    Autrewas purified by flash chromatography on silica gel

Mode opératoire

To a solution of 88 (240 mg, 1.45 mmol) in 7:3 CH2Cl2:MeOH (10 mL) was added TMS Diazomethane (2.0 M in hexanes) (0.9 mL, 1.8 mmol) in 0.2 ml aliquots until the color remained yellow. The reaction was allowed to stir for an additional 0.25 hours at room temperature. After stirring, glacial acetic acid was added dropwise until the solution became colorless. The reaction was concentrated in vacuo to an oil which was purified by flash chromatography on silica gel using ether:petroleum ether (1:9) to yield 89 (210 mg, 80%) as a clear oil. 1H NMR (CDCl3) δ 3.60 (s, 3H), 2.25-2.13 (m, 1H), 2.08-1.94 (m, 3H), 1.95-1.90 (m, 2H), 1.49-1.31 (m, 3H), 1.10-0.93 (m, 2H); 13C NMR (CDCl3) δ 176.7, 83.3, 69.8, 51.9, 43.4, 36.7, 31.9, 29.2, 26.3; APCI m/z (rel intensity) 181 (MH+, 100).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07989431B2uspto-grants-2011_08