3-(2-Bromoethyl)phenol → HCID 68872917、化合物
反応式
[Br:1][CH2:2][CH2:3][C:4]1[CH:5]=[C:6]([OH:10])[CH:7]=[CH:8][CH:9]=1>C(Cl)Cl>[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][C:4]([CH3:5])([CH3:9])[CH3:3])[CH:5]=1参加物
実験手順
3-(2-Bromoethyl)phenol (1.349 g, 6.709 mmol) in DCM (7 ml) was cooled under argon to −78° C. Under stirring, isobutene was bubbled into the mixture until more than 5 ml were added. Trifluoromethanesulphonic acid (50 μl) was dropped in. The mixture was stirred under argon at −78° C. for 4.5 hours. Triethylamine (120 μl) was added. The reaction mixture was allowed up to room temperature and then filtered. The filtrate was evaporated to dryness and petroleum ether (25 ml) was added into the residue. It was then filtered and evaporated. The obtained oil was solved in ethyl acetate, washed with water, dried (sodium sulphate) and evaporated. The residue was dissolved in CDCl3 and then evaporated. 1.223 g desired product was left, yield 71%.
後処理
- customisobutene was bubbled into the mixture until more than 5 ml
- additionwere added
- additionTrifluoromethanesulphonic acid (50 μl) was dropped in
- stirringThe mixture was stirred under argon at −78° C. for 4.5 hours
- additionTriethylamine (120 μl) was added
- customwas allowed up to room temperature
- filtrationfiltered
- customThe filtrate was evaporated to dryness and petroleum ether (25 ml)
- additionwas added into the residue
- filtrationIt was then filtered
- customevaporated
- washwashed with water
- dry with materialdried (sodium sulphate)
- customevaporated
- dissolutionThe residue was dissolved in CDCl3
- customevaporated
- wait1.223 g desired product was left
出典と根拠
- ORDレコード
- ord-dc53290d06f443b0b1787b9613f7fb1e
- 出典データセット
- uspto-grants-2009_04
- 特許番号
- US07521461B2
反応ノート
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