Hydrochloric Acid → 1-[2-(3-methylphenyl)-2H-tetrazol-5-yl]ethanone
反応式
C[Mg]Br.[CH2:4](N(CC)CC)C.[CH3:11][C:12]1[CH:13]=[C:14]([N:18]2[N:22]=[N:21][C:20]([C:23]([O:25]CC)=O)=[N:19]2)[CH:15]=[CH:16][CH:17]=1.Cl>C1(C)C=CC=CC=1.O>[CH3:11][C:12]1[CH:13]=[C:14]([N:18]2[N:22]=[N:21][C:20]([C:23](=[O:25])[CH3:4])=[N:19]2)[CH:15]=[CH:16][CH:17]=1参加物
反応条件
- 温度
- -10 °C
実験手順
Methylmagnesium bromide (1070 mL, 1.50 mol, 1.4 M in tetrahydrofuran/toluene) in triethylamine (520 mL, 3.74 mol) was added via an addition funnel to a stirred solution of ethyl 2-(3-methylphenyl)-2H-tetrazole-5-carboxylate in dry toluene (1000 mL) at −10° C. for 5 hours. The mixture was continued to stir at −10° C. overnight. A cooled (+3° C.) solution of hydrochloric acid (37%, 500 mL) and water (500 mL) was added over 2 hours 20 minutes. The layers were separated and the organic layer was washed with water (500 mL) and brine (2×250 mL). The aqueous layer was extracted with toluene (3×500 mL) and the toluene was washed with brine (2×250 mL). The combined organic extracts were concentrated and purified on silica using dichloromethane as eluent. The concentrated product residue was triturated with petroleum ether, filtrated and dried under reduced pressure at room temperature to give the title product (90.86 g, 60%).
後処理
- additionwas added over 2 hours 20 minutes
- customThe layers were separated
- washthe organic layer was washed with water (500 mL) and brine (2×250 mL)
- extractionThe aqueous layer was extracted with toluene (3×500 mL)
- washthe toluene was washed with brine (2×250 mL)
- concentrationThe combined organic extracts were concentrated
- custompurified on silica
- customThe concentrated product residue was triturated with petroleum ether
- filtrationfiltrated
- customdried under reduced pressure at room temperature
出典と根拠
- ORDレコード
- ord-7157c50a30df46abb3e7178b3cb58412
- 出典データセット
- uspto-grants-2011_06
- 特許番号
- US07960422B2
反応ノート
読み込み中…