tert-Butyl methyl ether → 3-(3,5-Dichloro-phenyl)-4,4,4-trifluoro-3-hydroxy-1-(4-methyl-5-trimethylsilanylethynyl-thiophen-2-yl)-butan-1-one

HRID 242401노트

반응식

HRID 242401 반응식
[H-].[Li+].[Cl:3][C:4]1[CH:5]=[C:6]([C:11](=[O:16])[C:12]([F:15])([F:14])[F:13])[CH:7]=[C:8]([Cl:10])[CH:9]=1.[CH3:17][C:18]1[CH:19]=[C:20]([C:29](=[O:31])[CH3:30])[S:21][C:22]=1[C:23]#[C:24][Si:25]([CH3:28])([CH3:27])[CH3:26].CC(OC)(C)C>C1COCC1>[Cl:3][C:4]1[CH:5]=[C:6]([C:11]([OH:16])([C:12]([F:13])([F:14])[F:15])[CH2:30][C:29]([C:20]2[S:21][C:22]([C:23]#[C:24][Si:25]([CH3:28])([CH3:26])[CH3:27])=[C:18]([CH3:17])[CH:19]=2)=[O:31])[CH:7]=[C:8]([Cl:10])[CH:9]=1

참가 물질

6

실험 절차

LiH (1.72 g) is added to a solution of 3′,5′-dichloro-2,2,2-trifluoroacetophenone (26.6 g) and 1-(4-methyl-5-trimethylsilanylethynyl-thiophen-2-yl)-ethanone (18.2 g) in THF (100 ml). After 30 minutes at 60° C. MTBE is added (200 ml) and the reaction mixture is poured onto water (30 ml) at 5° C. The organic phase is extracted with water and a saturated aqueous solution of NaCl, dried over Na2SO4 and concentrated in vacuo to yield 3-(3,5-dichloro-phenyl)-4,4,4-trifluoro-3-hydroxy-1-(4-methyl-5-trimethylsilanylethynyl-thiophen-2-yl)-butan-1-one (20.7 g). The crude product is used without further purification.

후처리

  1. additionthe reaction mixture is poured onto water (30 ml) at 5° C
  2. extractionThe organic phase is extracted with water
  3. dry with materiala saturated aqueous solution of NaCl, dried over Na2SO4
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-7264ff7c469b4bf4ad00d0bbb95e95ef
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08653116B2

반응 노트

불러오는 중…