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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Cesium carbonate → 1319255-41-8

HRID 589156
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반응식

HRID 589156 반응식
C([O-])([O-])=O.[Cs+].[Cs+].[F:7][CH2:8]Br.[CH3:10][C:11]1([CH3:25])[C:15]([CH3:17])([CH3:16])[O:14][B:13]([C:18]2[CH:23]=[CH:22][C:21]([OH:24])=[CH:20][CH:19]=2)[O:12]1>CC#N>[F:7][CH2:8][O:24][C:21]1[CH:20]=[CH:19][C:18]([B:13]2[O:14][C:15]([CH3:17])([CH3:16])[C:11]([CH3:25])([CH3:10])[O:12]2)=[CH:23][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10796Cesium carbonateHCID 61108BromofluoromethaneHCID 27346244-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

생성물 1

HCID 672949401319255-41-8

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Cs2CO3 (651.6 mg, 2.0 mmol) and then FCH2Br (446.6 mg, 4.0 mmol) were added to a mixture of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (220 mg, 1.0 mmol)) in CH3CN (10 ml). After stirring at room temperature overnight, the mixture was filtered and concentrated. Purification by column chromatography afforded 2-(4-(fluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane: LCMS tR=1.39 Min (5 min run, UV254nm). Mass calculated for, M+ 252.1, observed LC/MS m/z 253.1 (M+H).

후처리

  1. filtrationthe mixture was filtered
  2. concentrationconcentrated
  3. customPurification by column chromatography

출처 및 근거

ORD 기록
ord-15523f69464544838f1282c03a1934d2
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227971B2

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