반응 #955922

ord-702e323857614a30aa7e9a86c07e9c68

반응 방정식

Cc1cc(Cl)ccc1C(=O)O
4-Chloro-2-methylbenzoic acid
O=S(=O)(O)O
H2SO4
CO
MeOH
COC(=O)c1ccc(Cl)cc1C
methyl 4-chloro-2-methylbenzoate
수율 92.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was refluxed overnight
  2. 2
    기타MeOH was evaporated
  3. 3
    추출the residue was extracted with EtOAc
  4. 4
    건조dried over MgSO4
  5. 5
    여과filtered
  6. 6
    기타evaporated

실험 절차

4-Chloro-2-methylbenzoic acid (3 g, 17.6 mmol) was suspended in 12 ml of MeOH with 1 ml of concentrated H2SO4. The mixture was refluxed overnight, MeOH was evaporated and the residue was extracted with EtOAc, dried over MgSO4 filtered and evaporated to give methyl 4-chloro-2-methylbenzoate as a colorless viscous liquid (2.96 g, 92%) that was used in the next step without further purification. The ester (2.96 g, 16 mmol) was, under inert atmosphere, dissolved in THF (100 mL) and NMP (9 mL) and Iron (III) acetylacetonate (318 mg, 0.9 mmol) was added giving a red solution. Then EtMgBr (7 ml of 1M solution in ether) was added dropwise under vigorous stirring. The mixture turned dark brown and then violet and then was stirred for 15 more min. The reaction was diluted with ether and quenched upon the addition of aq. HCl (1M, 10 ml). The crude product was extracted with ether. The combined organic layers were washed with water and brine, dried over MgSO4 and evaporated. The residue was purified on silica gel (30% EtOAc/hexanes) to give methyl 4-ethyl-2-methylbenzoate as an oil (2.37 g, 83%). (1H NMR (500 MHz, CDCl3): δ 1.26 (t, 3H), 2.63 (dd, 2H), 3.9 (s, 3H), 7.1 (b, 2H), 7.85 (d, 1H)).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08968708B2uspto-grants-2015_03