反応 #3864789
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-8463ddfc864f4395a7ce85481e0390ce表示可能な構造データがありません
CCCCCCCCCCCCC(CCC)O製品情報
4-Hexadecanol (CAS 19781-43-2) 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 34541
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
11 反応 · 11 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8463ddfc864f4395a7ce85481e0390ce反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-hexadecanol; 3-hexadecanol; 4-hexadecanol;
ソース ID: ord-9d8370b7c81a4b7dba31e82777a09a8d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 4-Hexadecanol (12.29 g 0.051 mol) and p-Toluenesulfonyl chloride (12 g 0.063 mol) were dissolved Pyridine (100 ml) and stirred overnight at room temperature. Dichloromethane (400 ml) was added. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water, dried with anhydrous magnesium sulphate (10 g). After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water dried with anhydrous magnesium sulphate (10 g) After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained
ソース ID: ord-da09bdf779e241ce8305ad63b4c295a1反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 4-Hexadecanol (12.29 g 0.051 mol) and p-Toluenesulfonyl chloride (12 g 0.063 mol) were dissolved Pyridine (100 ml) and stirred overnight at room temperature. Dichloromethane (400 ml) was added. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water, dried with anhydrous magnesium sulphate (10 g). After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water dried with anhydrous magnesium sulphate (10 g) After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained
ソース ID: ord-da09bdf779e241ce8305ad63b4c295a1反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-hexadecanol; 3-hexadecanol; 4-hexadecanol;
ソース ID: ord-9d8370b7c81a4b7dba31e82777a09a8d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-hexadecanol; 3-hexadecanol; 4-hexadecanol;
ソース ID: ord-9d8370b7c81a4b7dba31e82777a09a8d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 4-Hexadecanol (12.29 g 0.051 mol) and p-Toluenesulfonyl chloride (12 g 0.063 mol) were dissolved Pyridine (100 ml) and stirred overnight at room temperature. Dichloromethane (400 ml) was added. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water, dried with anhydrous magnesium sulphate (10 g). After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water dried with anhydrous magnesium sulphate (10 g) After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained
ソース ID: ord-afa931a1bdb94d4aa05493a6545c8bb6反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 4-Hexadecanol (12.29 g 0.051 mol) and p-Toluenesulfonyl chloride (12 g 0.063 mol) were dissolved Pyridine (100 ml) and stirred overnight at room temperature. Dichloromethane (400 ml) was added. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water, dried with anhydrous magnesium sulphate (10 g). After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water dried with anhydrous magnesium sulphate (10 g) After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained
ソース ID: ord-afa931a1bdb94d4aa05493a6545c8bb6反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-hexadecanol; 3-hexadecanol; 4-hexadecanol;
ソース ID: ord-a096f9eab5c845ed832489e7b0053100反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 4-Hexadecanol (12.29 g 0.051 mol) and p-Toluenesulfonyl chloride (12 g 0.063 mol) were dissolved Pyridine (100 ml) and stirred overnight at room temperature. Dichloromethane (400 ml) was added. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water, dried with anhydrous magnesium sulphate (10 g). After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained. Dichloromethane solution was then washed well with water, H2SO4 (3%), water, NaHCO3 (3%) and water dried with anhydrous magnesium sulphate (10 g) After evaporation of the solvent 20 g of crude 4-Hexadecanesulfonyl chloride was obtained
ソース ID: ord-da09bdf779e241ce8305ad63b4c295a1反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-hexadecanol; 3-hexadecanol; 4-hexadecanol;
ソース ID: ord-9d8370b7c81a4b7dba31e82777a09a8dPubChem References
化合物の公開データベース記録に掲載された情報源です。
