反応式
[CH:1]([Mg]Br)([CH3:3])[CH3:2].Br[C:7]1[CH:16]=[C:15]([CH3:17])[CH:14]=[CH:13][C:8]=1[C:9]([O:11][CH3:12])=[O:10]>C1COCC1.Br[Zn]Br.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[CH:1]([C:7]1[CH:16]=[C:15]([CH3:17])[CH:14]=[CH:13][C:8]=1[C:9]([O:11][CH3:12])=[O:10])([CH3:3])[CH3:2]参加物
反応物 2
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- -48 °C
実験手順
To a stiffed mixture of dibromozinc (39.0 g, 173 mmol, 4.00 equiv) in THF (500 mL) under nitrogen at −48° C. was added dropwise isopropylmagnesium bromide (3 M in THF, 170 mmol) over a period of 30 min Pd(dppf)Cl2 (0.5 g, 0.05 equiv) and methyl 2-bromo-4-methylbenzoate (10.0 g, 43.7 mmol, 1.00 equiv) were added to the above reaction mixture. After stirring for 1 h at −48° C., the reaction mixture was quenched by the careful addition of 500 mL of NH4Cl (aq.). The resulting mixture was extracted with 3×500 mL of ethyl acetate. The combined organic layers were washed with 3×500 mL of brine and concentrated in vacuo. The residue was purified using silica gel column chromatography with petroleum ether (1:1) as eluent. This resulted in 6.50 g (77%) of methyl 2-isopropyl-4-methylbenzoate as a yellow oil.
後処理
- additionwere added to the above reaction mixture
- customthe reaction mixture was quenched by the careful addition of 500 mL of NH4Cl (aq.)
- extractionThe resulting mixture was extracted with 3×500 mL of ethyl acetate
- washThe combined organic layers were washed with 3×500 mL of brine
- concentrationconcentrated in vacuo
- customThe residue was purified
- customThis resulted in 6.50 g (77%) of methyl 2-isopropyl-4-methylbenzoate as a yellow oil
出典と根拠
- ORDレコード
- ord-20212813c911466ab351572052110faf
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08871790B2
関連ノート
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