反応 #4153868
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-6b23a0bf1c354236bdf37b8a426cd626表示可能な構造データがありません
CCCCOC(=O)C(C)OC1=CC=C(C=C1)O製品情報
butyl 2-(4-hydroxyphenoxy)propanoate (CAS 81947-94-6) 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 12919928
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
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6b23a0bf1c354236bdf37b8a426cd626反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-072c19a77fb64968bfc51f0b3617ff2d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-691ad8c3caf6439ea77b5b713cf5d017反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8ccb8617ef4e41eaa5eb25af6fd2956b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6b23a0bf1c354236bdf37b8a426cd626反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: While stirring a mixture of 25 g of (+)-butyl 2-(4-formylphenoxy)propionate ([α]D25 =+44.1°) and 75 g of toluene at room temperature, 22.8 g of 40% peracetic acid was dropwise added. After the reaction at 50° C. for 2 hours, the reaction mixture was subjected to liquid separation with an addition of water. The toluene layer was separated and washed with water. To the toluene layer, 25 g of sodium hydrogen carbonate and water was added, and the mixture was reacted at 50° C. for 5 hours. Then, the reaction mixture was subjected to liquid separation. The organic layer was washed twice with water. The organic layer was concentrated by distilling off toluene, and then subjected to distillation under reduced pressure, whereby 19.0 g of (+)-butyl 2-(4-hydroxyphenoxy)propionate was obtained as a colorless transparent liquid. The boiling point was 160° C./1 mmHg. After the reaction at 50° C. for 2 hours the reaction mixture was subjected to liquid separation with an addition of water The toluene layer was separated washed with water To the toluene layer, 25 g of sodium hydrogen carbonate and water was added the mixture was reacted at 50° C. for 5 hours Then, the reaction mixture was subjected to liquid separation The organic layer was washed twice with water The organic layer was concentrated by distilling off toluene subjected to distillation under reduced pressure
ソース ID: ord-7dc85adcff4049249fc9825ed4bdeb63反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: While stirring a mixture of 25 g of butyl 2-(4-formylphenoxy)propionate and 75 g of toluene at room temperature, 22.8 g of 40% peracetic acid was dropwise added. After stirring at 20° to 30° C. for 2 hours and at 50° C. for 2 hours, 2.0 g of water was added, and the mixture was stirred for 2 hours. The reaction mixture was cooled to room temperature and subjected to the same after-treatment as in Example 1, whereby 19.5 g of butyl 2-(4-hydroxyphenoxy)propionate was obtained as a colorless transparent liquid by the distillation under reduced pressure. The boiling point was 160° C./1 mmHg. After stirring at 20° to 30° C. for 2 hours and at 50° C. for 2 hours the mixture was stirred for 2 hours
ソース ID: ord-6a0b93ca6756416da6df04a6a83e6c27反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: While stirring a mixture of 25 g of butyl 2-(4-formylphenoxy)propionate and 75 g of toluene at room temperature, 22.8 g of 40% peracetic acid was dropwise added. After stirring at 20° to 30° C. for 2 hours and at 50° C. for 2 hours, 2.0 g of water was added, and the mixture was stirred for 2 hours. The reaction mixture was cooled to room temperature and subjected to the same after-treatment as in Example 1, whereby 19.5 g of butyl 2-(4-hydroxyphenoxy)propionate was obtained as a colorless transparent liquid by the distillation under reduced pressure. The boiling point was 160° C./1 mmHg. After stirring at 20° to 30° C. for 2 hours and at 50° C. for 2 hours the mixture was stirred for 2 hours
ソース ID: ord-6a0b93ca6756416da6df04a6a83e6c27反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-072c19a77fb64968bfc51f0b3617ff2d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-691ad8c3caf6439ea77b5b713cf5d017反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8ccb8617ef4e41eaa5eb25af6fd2956b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 121 g (1.1 moles) of hydroquinone were dissolved in 500 ml of dimethylsulfoxide, 37 g (0.5 mole) of calcium hydroxide were added to the solution, and the mixture was stirred for 1 hour at 45°-50° C. Thereafter, 82.3 g (0.455 mole) of optically active n-butyl 2-chloropropionate (αD20 =-13.0°) were added dropwise in the course of 1 hour at the same temperature. The mixture was stirred for a further 3 hours at 45°-50° C., cooled, and worked up as described in Example 1. 49.7 g (0.21 mole) of optically active n-butyl 2-(4-hydroxyphenoxy)-propionate were obtained. Yield: 46.2%; bp. =150°-152° C./0.22 mbar; αD20 =+11.8° ##STR7## The mixture was stirred for a further 3 hours at 45°-50° C. cooled
ソース ID: ord-86ee785db5494347bc7344a5c6d7d3ccPubChem 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。
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