4-Methyloxybenzyl chloride → Tert-butyl (3-bromo-2-chloro-5-(difluoromethyl)phenyl)(4-methoxybenzyl)carbamate

HRID 1430790ノート

反応式

HRID 1430790 の反応式
[Br:1][C:2]1[C:3]([Cl:19])=[C:4]([NH:11][C:12](=[O:18])[O:13][C:14]([CH3:17])([CH3:16])[CH3:15])[CH:5]=[C:6]([CH:8]([F:10])[F:9])[CH:7]=1.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[CH3:30][O:31][C:32]1[CH:39]=[CH:38][C:35]([CH2:36]Cl)=[CH:34][CH:33]=1.[Li+].[Cl-]>CN(C=O)C.CCOC(C)=O>[Br:1][C:2]1[C:3]([Cl:19])=[C:4]([N:11]([CH2:36][C:35]2[CH:38]=[CH:39][C:32]([O:31][CH3:30])=[CH:33][CH:34]=2)[C:12](=[O:18])[O:13][C:14]([CH3:15])([CH3:16])[CH3:17])[CH:5]=[C:6]([CH:8]([F:10])[F:9])[CH:7]=1

参加物

7

反応物 4

HCID 699934-Methyloxybenzyl chlorideHCID 433294Lithium ChlorideHCID 2724254Sodium bis(trimethylsilyl)amideHCID 86708469tert-Butyl (3-bromo-2-chloro-5-(difluoromethyl)phenyl)carbamate

生成物 1

HCID 86708468Tert-butyl (3-bromo-2-chloro-5-(difluoromethyl)phenyl)(4-methoxybenzyl)carbamate収率 94.2%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

tert-Butyl (3-bromo-2-chloro-5-(difluoromethyl)phenyl)carbamate (1.82 g, 5.10 mmol) was dissolved in DMF (11.1 mL) at room temperature. NaHMDS (6.12 mL, 6.12 mmol) was added dropwise and the reaction was stirred for 30 minutes before the addition of 4-methoxybenzyl chloride (0.904 mL, 6.64 mmol) and stirring overnight. The reaction mixture was diluted with EtOAc causing a ppt to form. 10% aq. LiCl solution was added and the two layers became clear with stirring. The mixture was poured into a separatory funnel and the organic layer was washed with an extra equivalent of 10% aq. LiCl solution. The organic layer was dried over Na2SO4 and concentrated. Column chromatography (220 g SiO2, 0 to 8% EtOAc-hexane, gradient elution) afforded the expected product tert-butyl (3-bromo-2-chloro-5-(difluoromethyl)phenyl)(4-methoxybenzyl)carbamate (2.29 g).

後処理

  1. customto form
  2. stirringwith stirring
  3. additionThe mixture was poured into a separatory funnel
  4. washthe organic layer was washed with an extra equivalent of 10% aq. LiCl solution
  5. dry with materialThe organic layer was dried over Na2SO4
  6. concentrationconcentrated
  7. washColumn chromatography (220 g SiO2, 0 to 8% EtOAc-hexane, gradient elution)

出典と根拠

ORDレコード
ord-0ac17ecd529646b5b1c22e93c3933171
出典データセット
uspto-grants-2015_01
特許番号
US08940736B2

反応ノート

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