反応 #4017862
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-16699d73cd344d77a4fea65a73c9295e表示可能な構造データがありません
CNCCS(=O)(=O)C1=CC=CC=C1製品情報
2-(benzenesulfonyl)-N-methylethanamine (CAS 61097-92-5) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 5152138
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
8 反応 · 8 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-16699d73cd344d77a4fea65a73c9295e反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 2-chloroethylphenyl sulfone and a large excess of methylamine (40% solution in water) in acetonitrile is stirred at room temperature overnight. The solvent is removed in vacuo and the residue is partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution is extracted with dilute sulfuric acid. The acidic extract is made basic with 50% sodium hydroxide and the basic solution is extracted with methylene chloride. The methylene chloride solution is dried over magnesium sulfate and the solvent is removed in vacuo to give the title compound. The solvent is removed in vacuo the residue is partitioned between methylene chloride and dilute sodium hydroxide The methylene chloride solution is extracted with dilute sulfuric acid The acidic extract the basic solution is extracted with methylene chloride The methylene chloride solution is dried over magnesium sulfate the solvent is removed in vacuo
ソース ID: ord-4bcb9985990d4f0a9ba58e9444d206e9反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 2-chloroethylphenyl sulfone and a large excess of methylamine (40% solution in water) in acetonitrile is stirred at room temperature overnight. The solvent is removed in vacuo and the residue is partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution is extracted with dilute sulfuric acid. The acidic extract is made basic with 50% sodium hydroxide and the basic solution is extracted with methylene chloride. The methylene chloride solution is dried over magnesium sulfate and the solvent is removed in vacuo to give the title compound. The solvent is removed in vacuo the residue is partitioned between methylene chloride and dilute sodium hydroxide The methylene chloride solution is extracted with dilute sulfuric acid The acidic extract the basic solution is extracted with methylene chloride The methylene chloride solution is dried over magnesium sulfate the solvent is removed in vacuo
ソース ID: ord-ae4c77ae86b04fcaa9012d4cce7a5a3a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-16699d73cd344d77a4fea65a73c9295e反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 2-chloroethylphenyl sulfone and a large excess of methylamine (40% solution in water) in acetonitrile is stirred at room temperature overnight. The solvent is removed in vacuo and the residue is partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution is extracted with dilute sulfuric acid. The acidic extract is made basic with 50% sodium hydroxide and the basic solution is extracted with methylene chloride. The methylene chloride solution is dried over magnesium sulfate and the solvent is removed in vacuo to give the title compound. The solvent is removed in vacuo the residue is partitioned between methylene chloride and dilute sodium hydroxide The methylene chloride solution is extracted with dilute sulfuric acid The acidic extract the basic solution is extracted with methylene chloride The methylene chloride solution is dried over magnesium sulfate the solvent is removed in vacuo
ソース ID: ord-ae4c77ae86b04fcaa9012d4cce7a5a3a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 2-chloroethylphenyl sulfone and a large excess of methylamine (40% solution in water) in acetonitrile is stirred at room temperature overnight. The solvent is removed in vacuo and the residue is partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution is extracted with dilute sulfuric acid. The acidic extract is made basic with 50% sodium hydroxide and the basic solution is extracted with methylene chloride. The methylene chloride solution is dried over magnesium sulfate and the solvent is removed in vacuo to give the title compound. The solvent is removed in vacuo the residue is partitioned between methylene chloride and dilute sodium hydroxide The methylene chloride solution is extracted with dilute sulfuric acid The acidic extract the basic solution is extracted with methylene chloride The methylene chloride solution is dried over magnesium sulfate the solvent is removed in vacuo
ソース ID: ord-4bcb9985990d4f0a9ba58e9444d206e9反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-16699d73cd344d77a4fea65a73c9295e反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 2-chloroethylphenyl sulfone and a large excess of methylamine (40% solution in water) in acetonitrile is stirred at room temperature overnight. The solvent is removed in vacuo and the residue is partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution is extracted with dilute sulfuric acid. The acidic extract is made basic with 50% sodium hydroxide and the basic solution is extracted with methylene chloride. The methylene chloride solution is dried over magnesium sulfate and the solvent is removed in vacuo to give the title compound. The solvent is removed in vacuo the residue is partitioned between methylene chloride and dilute sodium hydroxide The methylene chloride solution is extracted with dilute sulfuric acid The acidic extract the basic solution is extracted with methylene chloride The methylene chloride solution is dried over magnesium sulfate the solvent is removed in vacuo
ソース ID: ord-ae4c77ae86b04fcaa9012d4cce7a5a3aPubChem References
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