反応式
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[OH:11])([CH3:4])([CH3:3])[CH3:2].C1C(=O)N([Br:19])C(=O)C1>CC#N>[C:1]([C:5]1[CH:10]=[C:9]([Br:19])[CH:8]=[CH:7][C:6]=1[OH:11])([CH3:4])([CH3:2])[CH3:3]参加物
4
実験手順
To a solution of 2-tert-butylphenol (250 g, 1.67 mol) in CH3CN (1500 mL) was added NBS (300 g, 1.67 mol) at room temperature. After addition, the mixture was stirred at room temperature overnight and then the solvent was removed. Petroleum ether (1000 mL) was added, and the resulting white precipitate was filtered off. The filtrate was concentrated under reduced pressure to give the crude 2-tert-butyl-4-bromophenol (380 g), which was used without further purification.
後処理
- additionAfter addition
- customthe solvent was removed
- additionPetroleum ether (1000 mL) was added
- filtrationthe resulting white precipitate was filtered off
- concentrationThe filtrate was concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-97ca45fe2d5043acb3e89dba7009a4e9
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08829204B2
関連ノート
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