Methanol → Chenodeoxycholic Acid

HRID 2199017노트

반응식

HRID 2199017 반응식
CO.[OH-].[K+].C([O:8][C@@H:9]1[CH2:33][CH2:32][C@@:31]2([CH3:34])[C@H:11]([CH2:12][C@@H:13]([O:36]C(=O)C)[C@@H:14]3[C@@H:30]2[CH2:29][CH2:28][C@@:27]2([CH3:35])[C@H:15]3[CH2:16][CH2:17][C@@H:18]2[C@H:19]([CH3:26])[CH2:20][CH2:21][C:22]([O:24]C)=[O:23])[CH2:10]1)(=O)C>C(O)(C)C>[CH3:26][C@@H:19]([C@@H:18]1[C@@:27]2([CH3:35])[CH2:28][CH2:29][C@@H:30]3[C@@:31]4([CH3:34])[CH2:32][CH2:33][C@@H:9]([OH:8])[CH2:10][C@H:11]4[CH2:12][C@@H:13]([OH:36])[C@H:14]3[C@@H:15]2[CH2:16][CH2:17]1)[CH2:20][CH2:21][C:22]([OH:24])=[O:23]

참가 물질

5

실험 절차

To a solution of 3 ml of methanol, 5 ml of isopropanol and 0.8 g of potassium hydroxide was added 0.294 g (0.000599 mol) of methyl 3α,7α-diacetyloxy-5β-cholan-24-oate. The mixture was heated to reflux under an argon atmosphere for 4 hr. then stirred overnight at room temperature. The solvents were removed in vacuo. The mixture was acidified with 1 N HCl and extracted with 3×25 ml of ethyl acetate. The combined ethyl acetate extracts were washed with water then dried over anhydrous sodium sulfate. The mixture was filtered and solvents removed in vacuo. The residue were recrystallized from ethyl acetate to give 0.163 g (69.3%) of chenodeoxycholic acid, mp 117°-118° C., which did not depress when mixed with authentic material (mp 117°-118° C. from ethyl acetate).

후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux under an argon atmosphere for 4 hr
  3. customThe solvents were removed in vacuo
  4. extractionextracted with 3×25 ml of ethyl acetate
  5. washThe combined ethyl acetate extracts were washed with water
  6. dry with materialthen dried over anhydrous sodium sulfate
  7. filtrationThe mixture was filtered
  8. customsolvents removed in vacuo
  9. customThe residue were recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-0d6f9aefa3fb4505af7c0c11c2748644
출처 데이터셋
uspto-grants-1982_11
특허 번호
US04360470

반응 노트

불러오는 중…