Clofibric Acid → Fibric acid

HRID 327623

반응식

HRID 327623 반응식
Cl[C:2]1[CH:14]=[CH:13][C:5]([O:6][C:7]([CH3:12])([CH3:11])[C:8]([OH:10])=[O:9])=[CH:4][CH:3]=1.[OH-].[K+]>CO.O1CCOCC1.O.[Ni]>[O:6]([C:7]([CH3:12])([CH3:11])[C:8]([OH:10])=[O:9])[C:5]1[CH:13]=[CH:14][CH:2]=[CH:3][CH:4]=1

참가 물질

7

실험 절차

To a solution of 20.0 g (0.93 mole) of 2-(4-chlorophenoxy)-2-methylpropionic acid (97%, clofibric acid, Aldrich) in 130 ml of methanol and 50 ml of dioxane was added a solution of 13.9 g (0.244 mole) of potassium hydroxide in 75 ml of water. To this solution were added 5 teaspoonfuls of Raney Nickel (Aldrich) and the mixture was hydrogenated at ambient temperature for 3.25 hr (H2 -uptake ceased). The reaction mixture was filtered through Celite® and the filtrate was concentrated under reduced pressure to a volume of 150 ml. This solution was extracted with 200 ml of ethyl ether and the ether was discarded. The aqueous layer pH was adjusted to 2 with concentrated hydrochloric acid solution and the resulting white solid was collected by filtration and dried to give 16 g (99%) of white solid. An analytical sample was prepared by recrystallizing from cyclohexane-petroleum ether (b.p. range 30°-60° C.) to give white crystals, mp 98°-100° C.

후처리

  1. filtrationThe reaction mixture was filtered through Celite®
  2. concentrationthe filtrate was concentrated under reduced pressure to a volume of 150 ml
  3. extractionThis solution was extracted with 200 ml of ethyl ether
  4. filtrationthe resulting white solid was collected by filtration
  5. customdried

출처 및 근거

ORD 기록
ord-b70d0fb132884df6ac5ea9b62b7ae345
출처 데이터셋
uspto-grants-1993_12
특허 번호
US05273993

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