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

HRID 1842900
ノート
印刷プレビュー

反応式

HRID 1842900 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 25517Ammonium ChlorideHCID 113453114-Bromo-2-fluoro-benzoic acid methyl esterHCID 178461634HCID 178461634、化合物

生成物 1

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

試薬・触媒・溶媒 2

HCID 178460666HCID 178460666、化合物触媒HCID 3283
Diethyl Ether
溶媒
2 回

反応条件

温度
-78 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-d3e02c0a2c4046c386ea68452455d3ad
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08946204B2

反応ノート

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