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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-(1,1,1-Trifluoro-2-hydroxypropan-2-yl)phenol → 4-(2-Hydroxy-1,1,1-trifluoro-2-propyl)cyclohexanol

HRID 1419794
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인쇄 미리보기

반응식

HRID 1419794 반응식
[OH:1][C:2]([C:8]1[CH:13]=[CH:12][C:11]([OH:14])=[CH:10][CH:9]=1)([CH3:7])[C:3]([F:6])([F:5])[F:4]>C(O)(C)C.Cl.[Rh]>[OH:1][C:2]([CH:8]1[CH2:13][CH2:12][CH:11]([OH:14])[CH2:10][CH2:9]1)([CH3:7])[C:3]([F:4])([F:5])[F:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 544399464-(1,1,1-Trifluoro-2-hydroxypropan-2-yl)phenol

생성물 1

HCID 539089674-(2-Hydroxy-1,1,1-trifluoro-2-propyl)cyclohexanol

시약·촉매·용매 3

HCID 23948Rhodium촉매HCID 313Hydrochloric Acid용매HCID 3776Isopropanol용매

실험 절차

18.9 g (0.092 mol) of 4-(2-hydroxy-1,1,1-trifluoro-2-propyl)phenol were hydrogenated in a mixture of 200 ml of isopropanol and 6 ml of concentrated hydrochloric acid in the presence of 2.3 g of rhodium (5% on charcoal) at 150 bar and 50° C. After filtration to remove the catalyst and concentration, 18.8 g (96.6% of theory) remained of a colorless product.

후처리

  1. filtrationAfter filtration
  2. customto remove
  3. concentrationthe catalyst and concentration, 18.8 g (96.6% of theory)

출처 및 근거

ORD 기록
ord-d0d4752887c24f14bb1f64ec4d666a79
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05889012

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