홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

(2-Bromo-4-phenylphenyl) acetate → 3-Bromo-4'-hydroxybiphenyl

HRID 1493837
노트
인쇄 미리보기

반응식

HRID 1493837 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:12]2[CH:17]=[CH:16]C=[CH:14][CH:13]=2)[CH:5]=[CH:6][C:7]=1OC(=O)C.[CH3:18][O-:19].[Na+]>CO>[Br:1][C:2]1[CH:3]=[C:4]([C:12]2[CH:17]=[CH:16][C:18]([OH:19])=[CH:14][CH:13]=2)[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 346071(2-Bromo-4-phenylphenyl) acetateHCID 10942334Sodium Methoxide

생성물 1

HCID 156615023-Bromo-4'-hydroxybiphenyl

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a stirred solution of 1.07 g (3.67 mmole) of 3-bromo-4-acetoxybiphenyl in 10 mL methanol at ambient temperature under a nitrogen atmosphere was added 0.92 mL of 4.4 M sodium methoxide in methanol solution (4 mmole). The mixture was stirred for 20 minutes and partitioned between Et2O/ice-H2O/2N HCl (aq.) and the organic phase separated, washed with saturated NaCl solution, and then ice-H2O/saturated NaHCO3 (aq) solution, dried over Na2SO4, filtered, and evaporated. The product was dried in vacuo to give 1.05 g of crude 3-bromo-4'-hydroxybiphenyl which was used without further purification.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. custompartitioned between Et2O/ice-H2O/2N HCl (aq.)
  2. customthe organic phase separated
  3. washwashed with saturated NaCl solution
  4. dry with materialice-H2O/saturated NaHCO3 (aq) solution, dried over Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe product was dried in vacuo

출처 및 근거

ORD 기록
ord-370916984d394ca7a92863db4c9bb072
출처 데이터셋
uspto-grants-1991_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05025006

반응 노트

불러오는 중…