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1-triphenylmethyl-4-[2-(4-trifluoromethylphenoxy)ethyl]-1H-imidazole → HCID 178506221, 화합물

HRID 726263
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인쇄 미리보기

반응식

HRID 726263 반응식
C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:8]2[CH:12]=[C:11]([CH2:13][CH2:14][O:15][C:16]3[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=3)[N:10]=[CH:9]2)C=CC=CC=1>O1CCCC1.Cl>[F:25][C:22]([F:23])([F:24])[C:19]1[CH:20]=[CH:21][C:16]([O:15][CH2:14][CH2:13][C:11]2[N:10]=[CH:9][NH:8][CH:12]=2)=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 107439231-triphenylmethyl-4-[2-(4-trifluoromethylphenoxy)ethyl]-1H-imidazole

생성물 1

HCID 178506221HCID 178506221, 화합물

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 640 mg (1.28 mmol) of 1-triphenylmethyl-4-[2-(4-trifluoromethylphenoxy)ethyl]-1H-imidazole in 2 ml of tetrahydrofuran and 5 ml of 2N hydrochloric acid is heated at 70° C. for 2 hours. The tetrahydrofuran is then evaporated under reduced pressure and the residue extracted with diethyl ether. The aqueous solution is basified with potassium carbonate and the white solid is filtered and washed 3 times with water to give the title compound, M.p.: 105°-109° C.

후처리

  1. customThe tetrahydrofuran is then evaporated under reduced pressure
  2. extractionthe residue extracted with diethyl ether
  3. filtrationthe white solid is filtered
  4. washwashed 3 times with water

출처 및 근거

ORD 기록
ord-ab0787d6f51340fca9fb41d2840677ec
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05708171

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