反応式
[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([OH:9])=[C:4]([CH3:10])[CH:3]=1.[Br:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]Br.C(=O)([O-])[O-].[K+].[K+].O>CN(C)C=O.C(Cl)Cl>[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([O:9][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][Br:11])=[C:4]([CH3:10])[CH:3]=1参加物
実験手順
A solution of 4-bromo-2,6-dimethylphenol (2.00 g) and 1,7-dibromoheptane (5.10 g) in N,N-dimethylformamide (20 ml) was treated with potassium carbonate (2.06 g), and the mixture was stirred for 5 hours at ambient temperature. To the reaction mixture was added water and methylene chloride, and the organic layer was separated and dried over magnesium sulfate. Magnesium sulfate was filtered off, and the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography eluting successively with the following solvents: (1) n-hexane, (2) n-hexane:ethyl acetate=4:1, (3) n-hexane:ethyl acetate=1:1. The fractions containing the object compound were concentrated in vacuo to give crude 5-bromo-2-(7-bromoheptyloxy)-1,3-dimethylbenzene, that was used in the next reaction directly, as a pale yellow oil.
後処理
- customthe organic layer was separated
- dry with materialdried over magnesium sulfate
- filtrationMagnesium sulfate was filtered off
- concentrationthe filtrate was concentrated in vacuo
- customThe residue was purified by silica gel column chromatography
- washeluting successively with the following solvents
- additionThe fractions containing the object compound
- concentrationwere concentrated in vacuo
出典と根拠
- ORDレコード
- ord-7fc2b0d85ff048f1a19a243b72b12415
- 出典データセット
- uspto-grants-2005_04
- 特許番号
- US06884868B1
関連ノート
読み込み中…