Pyridine → 4-(3-Methyl-5-phenyl-pentyloxycarbonyloxy)-undecanoic acid 2-naphthalen-2-yl-2-oxo-ethyl ester

HRID 1384415노트

반응식

HRID 1384415 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11](=[O:27])[CH2:12][O:13][C:14](=[O:26])[CH2:15][CH2:16][CH:17]([OH:25])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24].N1C=CC=CC=1.[CH3:34][CH:35]([CH2:39][CH2:40][C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1)[CH2:36][CH2:37][OH:38].Cl[C:48]([O-])=[O:49]>C1COCC1>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11](=[O:27])[CH2:12][O:13][C:14](=[O:26])[CH2:15][CH2:16][CH:17]([O:25][C:48]([O:38][CH2:37][CH2:36][CH:35]([CH3:34])[CH2:39][CH2:40][C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1)=[O:49])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]

참가 물질

5

실험 절차

To a solution of 4.00 g of 4-hydroxy-undecanoic acid-2-naphthalen-2-yl-2-oxo-ethyl ester and 1.71 g of pyridine in 20 ml of THF, a solution of 2.91 g of 3-methyl-5-phenyl-pentanol-chloroformate in 10 ml of THF was dropped in at 0° C. The mixture was stirred for 3 hours at room temperature. Then, the reaction mixture was quenched with water and extracted with ether. The organic phase was washed with 2N HCl, saturated sodium bicarbonate, and water. Then, the mixture was dried, filtered, and evaporated to dryness. The resulting yellow oil was purified by chromatography to yield 5.46 g of a colorless oil.

후처리

  1. customThen, the reaction mixture was quenched with water
  2. extractionextracted with ether
  3. washThe organic phase was washed with 2N HCl, saturated sodium bicarbonate, and water
  4. customThen, the mixture was dried
  5. filtrationfiltered
  6. customevaporated to dryness
  7. customThe resulting yellow oil was purified by chromatography

출처 및 근거

ORD 기록
ord-d7e18d01bfdf4e978b73d821399304bc
출처 데이터셋
uspto-grants-2001_07
특허 번호
US06258854B1

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