Sodium Hydroxide → (1r,2s,4r)-2-Hydroxy-4-methylcyclohexanecarboxylic acid

HRID 1015657노트

반응식

HRID 1015657 반응식
C[O:2][C:3]([C@@H:5]1[CH2:10][CH2:9][C@@H:8]([CH3:11])[CH2:7][C@@H:6]1[OH:12])=[O:4].[OH-].[Na+]>CO>[OH:12][C@H:6]1[CH2:7][C@H:8]([CH3:11])[CH2:9][CH2:10][C@H:5]1[C:3]([OH:4])=[O:2]

참가 물질

4

반응 조건

온도
50 °C

실험 절차

To a solution of (1R,2S,4R)-2-Hydroxy-4-methyl-cyclohexanecarboxylic acid methyl ester (450 mg, 2.42 mmol) in methanol (12 ml) was added a 2.5 M solution of sodium hydroxide (9.7 ml, 24.2 mmol). The reaction mixture was stirred for 4 h at 50° C. Then, the solvents were removed and the residue was partitioned between 20 ml of H2O acidified to pH 4 and 20 ml of EtOAc. The organic layer was separated and the aqueous phase was washed with ethyl acetate (2×20 ml). The combined ethyl acetate layers were dried (Na2SO4) and concentrated to obtain 313 mg (82%) of (1R,2S,4R)-2-Hydroxy-4-methyl-cyclohexanecarboxylic acid. NMR 1H (CDCl3, 400 MHz) 4.34 ppm (s, 1H); 2.43-2.39 ppm (m, 1H); 1.96-1.76 ppm (m, 5H); 1.14-1.08 ppm (m, 1H); 1.02-0.93 ppm (m, 1H); 0.90 ppm (d, 3H).

후처리

  1. customThen, the solvents were removed
  2. customthe residue was partitioned between 20 ml of H2O
  3. customThe organic layer was separated
  4. washthe aqueous phase was washed with ethyl acetate (2×20 ml)
  5. dry with materialThe combined ethyl acetate layers were dried (Na2SO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1396eca061054da4b3292c7544d540a9
출처 데이터셋
uspto-grants-2011_07
특허 번호
US07985769B2

반응 노트

불러오는 중…