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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-(2,4-Difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → 3'-Bromo-5'-tert-butyl-2,4-difluoro-4'-methoxybiphenyl

HRID 530654
노트
인쇄 미리보기

반응식

HRID 530654 반응식
[Br:1][C:2]1[CH:7]=[C:6](I)[CH:5]=[C:4]([C:9]([CH3:12])([CH3:11])[CH3:10])[C:3]=1[O:13][CH3:14].CC1(C)C(C)(C)OB([C:23]2[CH:28]=[CH:27][C:26]([F:29])=[CH:25][C:24]=2[F:30])O1>>[Br:1][C:2]1[CH:7]=[C:6]([C:23]2[CH:28]=[CH:27][C:26]([F:29])=[CH:25][C:24]=2[F:30])[CH:5]=[C:4]([C:9]([CH3:12])([CH3:11])[CH3:10])[C:3]=1[O:13][CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 162176522-(2,4-Difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 667000451-Bromo-3-tert-butyl-5-iodo-2-methoxybenzene

생성물 1

HCID 668338233'-Bromo-5'-tert-butyl-2,4-difluoro-4'-methoxybiphenyl

실험 절차

The product from Example 1 Part A (0.185 g, 0.501 mmol) and 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,5-difluorobenzene (0.120 g, 0.501 mmol) were reacted in the same manner as Example 1 Part B for 16 hours. The crude product was purified on an Isco 12 g silica cartridge eluting with 5% ethyl acetate in hexane to give the title compound.

후처리

  1. customThe crude product was purified on an Isco 12 g silica cartridge
  2. washeluting with 5% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-8f2f4bb5028c43e2a6410ce8fc4139f4
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353091B2

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