Methanol → Methyl 2,4,6-trimethylbenzene-1-sulfonate
反応式
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[C:3]=1[S:10](Cl)(=[O:12])=[O:11].[OH-:14].[Na+].[CH3:16]O>>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[C:3]=1[S:10]([O:12][CH3:16])(=[O:14])=[O:11]参加物
4
実験手順
to a solution of 2,4,6-trimethylbenzene-1-sulfonyl chloride (30 g, 0.136 mol) dissolved in methanol (350 ml), a solution of NaOH (5.49 g, 0.136 mol, 1 equiv.) dissolved in methanol (60 ml) was added dropwise. White NaCl was precipitated and filtered to remove NaCl, and the filtered solution was evaporated, followed by extraction with water and methylene chloride, and the organic layer was obtained, evaporated the solvent therefrom and then dried in a vacuum, affording a white solid at a yield of 96%.
後処理
- additionwas added dropwise
- customWhite NaCl was precipitated
- filtrationfiltered
- customto remove NaCl
- customthe filtered solution was evaporated
- extractionfollowed by extraction with water and methylene chloride
- customthe organic layer was obtained
- customevaporated the solvent
- customdried in a vacuum
- customaffording a white solid at a yield of 96%
出典と根拠
- ORDレコード
- ord-7c0eebe1760e4946aaf165df84aa45b7
- 出典データセット
- uspto-grants-2015_06
- 特許番号
- US09057929B2
反応ノート
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