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Methanol → Methyl 3-bromo-5-ethylbenzoate

HRID 1397262
ノート
印刷プレビュー

反応式

HRID 1397262 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([CH2:11][CH3:12])[CH:10]=1)[C:5]([OH:7])=[O:6].O=S(Cl)Cl.[CH3:17]O>>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([CH2:11][CH3:12])[CH:10]=1)[C:5]([O:7][CH3:17])=[O:6]
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

4

反応物 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 8260993-Bromo-5-ethylbenzoic acid

生成物 1

HCID 67325611Methyl 3-bromo-5-ethylbenzoate収率 92%

反応条件

温度
0 °C

実験手順

The compound 3-bromo-5-ethylbenzoic acid (0.95 g, 4.14 mmol) was dissolved in MeOH (50 mL), reaction mixture was cooled to 0° C. and SOCl2 (0.5 mL) was added. The reaction mixture was allowed to stir at room temperature for 10 h. The reaction mixture was concentrated under reduced pressure and diluted with CH2Cl2. The organic layer was washed with 10% NaHCO3 solution, water and brine. The organic phase was dried over anhydrous sodium sulfate and solvent was removed under reduced pressure. Methyl 3-bromo-5-ethylbenzoate (0.92 g, yield 92%) was isolated as colorless liquid and carried through without further purification. 1H NMR (300 MHz, CDCl3) δ 7.99 (t, J=1.6 Hz, 1H), 7.81 (d, J=1.4 Hz, 1H), 7.54 (t, J=1.6 Hz, 1H), 3.92 (s, 3H), 2.69 (q, J=7.6 Hz, 2H), 1.26 (t, J=7.6 Hz, 3H).

後処理

  1. customreaction mixture
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additiondiluted with CH2Cl2
  4. washThe organic layer was washed with 10% NaHCO3 solution, water and brine
  5. dry with materialThe organic phase was dried over anhydrous sodium sulfate and solvent
  6. customwas removed under reduced pressure

出典と根拠

ORDレコード
ord-4fde1fafff39434ab3c31fa7bdefa708
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08901156B2

反応ノート

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