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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trimethyl borate → 3-Fluoro-5-(4-fluorophenoxy)phenylboronic acid

HRID 1078230
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인쇄 미리보기

반응식

HRID 1078230 반응식
[F:1][C:2]1[CH:3]=[C:4](Br)[CH:5]=[C:6]([O:8][C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)[CH:7]=1.C([Li])CCC.[B:22](OC)([O:25]C)[O:23]C>O1CCCC1>[F:1][C:2]1[CH:3]=[C:4]([B:22]([OH:25])[OH:23])[CH:5]=[C:6]([O:8][C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8470Trimethyl borateHCID 197072103-Fluoro-5-(4-fluorophenoxy)phenyl bromideHCID 178418339Butyllithium

생성물 1

HCID 197072063-Fluoro-5-(4-fluorophenoxy)phenylboronic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

This compound is prepared in a manner analogous to that of Step B of Example 6, using 9.1 grams (0.032 mole) of 3-fluoro-5-(4-fluorophenoxy)phenyl bromide, 14 mL (0.035 mole) of n-butyllithium (2.5M in hexanes), and 10.4 mL (0.095 mole) of trimethyl borate in 100 mL of tetrahydrofuran, yielding 3-fluoro-5-(4-fluorophenoxy)phenylboronic acid.

후처리

  1. customThis compound is prepared in a manner analogous to that of Step B of Example 6

출처 및 근거

ORD 기록
ord-ea1b1ffeaa6b4e93a6f18d94fbf9366a
출처 데이터셋
uspto-grants-1996_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05547954

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