HCID 21556730、化合物 → HCID 21556745、化合物
反応式
[O-:1]I(=O)(=O)=O.[Na+].[CH3:7][S:8][C:9]1[CH:14]=[C:13]([CH:15]([CH3:17])[CH3:16])[C:12]([Br:18])=[CH:11][C:10]=1[CH:19]([CH3:21])[CH3:20]>O.CO.CC(C)=O>[CH3:7][S:8]([C:9]1[CH:14]=[C:13]([CH:15]([CH3:16])[CH3:17])[C:12]([Br:18])=[CH:11][C:10]=1[CH:19]([CH3:21])[CH3:20])=[O:1]参加物
実験手順
4-Bromo-2,5-diisopropylphenyl methyl sulfoxide was prepared as follows: A solution of 25.7 g of sodium m-periodate in 200 ml of water was added portionwise over 0.5 hour to 31.9 g of 4-bromo-2,5-diisopropylphenyl methyl sulfide (prepared in Example 1C) in 200 ml of methanol and 350 ml of acetone at ambient temperature. After stirring for 16 hours, the reaction mixture was filtered and the solid portion was extracted with chloroform. The filtrate was diluted with 1 liter of water and the solid residue that formed was collected on a filter. The second residue was extracted with chloroform. The two chloroform extracts were combined, washed with half-saturated sodium chloride solution, and dried over sodium sulfate. Removal of the chloroform gave a pale-yellow product containing some sulfide which was removed by recrystallization from n-hexane to give pure 4-bromo-2,5-diisopropylphenyl methyl sulfoxide which softened at 110°C and melted at 114°-117°C [Ʊ(S=O) 9.6μ].
後処理
- custom4-Bromo-2,5-diisopropylphenyl methyl sulfoxide was prepared
- filtrationthe reaction mixture was filtered
- extractionthe solid portion was extracted with chloroform
- additionThe filtrate was diluted with 1 liter of water
- customthe solid residue that formed
- customwas collected on a filter
- extractionThe second residue was extracted with chloroform
- washwashed with half-saturated sodium chloride solution
- dry with materialdried over sodium sulfate
- customRemoval of the chloroform
- customgave a pale-yellow product
- customwas removed by recrystallization from n-hexane
出典と根拠
- ORDレコード
- ord-3e5f0e7bdda741cbbd96713499ae4618
- 出典データセット
- uspto-grants-1976_03
- 特許番号
- US03941826
反応ノート
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