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

Ammonium Chloride → 1-(4-Bromo-2-fluorophenyl)cyclopropan-1-ol

HRID 1842900
노트
인쇄 미리보기

반응식

HRID 1842900 반응식
[CH2:1]([Mg]I)[CH3:2].[Br:5][C:6]1[CH:15]=[CH:14][C:9]([C:10]([O:12]C)=O)=[C:8]([F:16])[CH:7]=1.[NH4+].[Cl-]>C(OCC)C.CC(O[Ti](OC(C)C)(OC(C)C)OC(C)C)C>[Br:5][C:6]1[CH:15]=[CH:14][C:9]([C:10]2([OH:12])[CH2:2][CH2:1]2)=[C:8]([F:16])[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 25517Ammonium ChlorideHCID 113453114-Bromo-2-fluoro-benzoic acid methyl esterHCID 178461634HCID 178461634, 화합물

생성물 1

HCID 626689571-(4-Bromo-2-fluorophenyl)cyclopropan-1-ol수율 28%

시약·촉매·용매 2

HCID 178460666HCID 178460666, 화합물촉매HCID 3283
Diethyl Ether
용매
2회

반응 조건

온도
-78 °C

실험 절차

To a stirred solution of Ti(OiPr)4 (44.68 mL, 141.63 mmol, 1 eq) in diethyl ether (250 mL) was added freshly prepared ethyl magnesium iodide (212.44 mL, 424.89 mmol, 3 eq) in diethyl ether (220 mL) at −78° C. for 45 min. The reaction mixture was stirred for 90 min at −78° C., then methyl 4-bromo-2-fluorobenzoate (33.0 g, 141.63 mmol, 1.0 eq) was added and the mixture allowed to stir at RT for 16 h. Saturated aqueous NH4Cl (30 mL) was added and the mixture passed through celite pad. The ether layer was separated, washed with 1 N HCl (250 mL), brine (500 mL), water (750 mL), dried over MgSO4 and the solvent evaporated. The resulting residue was purified by CC using PE/EtOAc (19:1) as eluent to get 1-(4-bromo-2-fluorophenyl)cyclopropanol (9.01 g, 28%; TLC system: PE/EtOAc (9:1), Rf: 0.3).

후처리

  1. stirringto stir at RT for 16 h
  2. customThe ether layer was separated
  3. washwashed with 1 N HCl (250 mL), brine (500 mL), water (750 mL)
  4. dry with materialdried over MgSO4
  5. customthe solvent evaporated
  6. customThe resulting residue was purified by CC

출처 및 근거

ORD 기록
ord-d3e02c0a2c4046c386ea68452455d3ad
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946204B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트