反応 #4149291
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-41301d12f6474a56967d63c95673e497表示可能な構造データがありません
COC1=CC=CC=C1NC(=S)N製品情報
(2-methoxyphenyl)thiourea (CAS 1516-37-6) 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 722774
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
6 反応 · 6 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-41301d12f6474a56967d63c95673e497反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-41301d12f6474a56967d63c95673e497反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To 50 ml of acetone were added 2.46 g of o-anisidine and 3.75 g of benzoyl isothiocyanate, and the mixture is stirred under reflux for 2 hours and, then, allowed to stand overnight in a refrigerator at 5° C. The resulting crystals were collected by filtration, washed with cold acetone and dried under reduced pressure. The crystals were added to 50 ml of 30% methylamine-methanol and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated to dryness under reduced pressure, and the residue was washed with ethanol-ethyl acetate and dried under reduced pressure. The procedure provided 2.08 g of N-(o-methoxyphenyl)thiourea. under reflux for 2 hours The resulting crystals were collected by filtration washed with cold acetone dried under reduced pressure The crystals were added to 50 ml of 30% methylamine-methanol the mixture was stirred at room temperature overnight The reaction mixture was concentrated to dryness under reduced pressure the residue was washed with ethanol-ethyl acetate dried under reduced pressure
ソース ID: ord-de9bab9b5e424189ac8c17363b982488反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To 50 ml of acetone were added 2.46 g of o-anisidine and 3.75 g of benzoyl isothiocyanate, and the mixture is stirred under reflux for 2 hours and, then, allowed to stand overnight in a refrigerator at 5° C. The resulting crystals were collected by filtration, washed with cold acetone and dried under reduced pressure. The crystals were added to 50 ml of 30% methylamine-methanol and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated to dryness under reduced pressure, and the residue was washed with ethanol-ethyl acetate and dried under reduced pressure. The procedure provided 2.08 g of N-(o-methoxyphenyl)thiourea. under reflux for 2 hours The resulting crystals were collected by filtration washed with cold acetone dried under reduced pressure The crystals were added to 50 ml of 30% methylamine-methanol the mixture was stirred at room temperature overnight The reaction mixture was concentrated to dryness under reduced pressure the residue was washed with ethanol-ethyl acetate dried under reduced pressure
ソース ID: ord-de9bab9b5e424189ac8c17363b982488反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To 50 ml of acetone were added 2.46 g of o-anisidine and 3.75 g of benzoyl isothiocyanate, and the mixture is stirred under reflux for 2 hours and, then, allowed to stand overnight in a refrigerator at 5° C. The resulting crystals were collected by filtration, washed with cold acetone and dried under reduced pressure. The crystals were added to 50 ml of 30% methylamine-methanol and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated to dryness under reduced pressure, and the residue was washed with ethanol-ethyl acetate and dried under reduced pressure. The procedure provided 2.08 g of N-(o-methoxyphenyl)thiourea. under reflux for 2 hours The resulting crystals were collected by filtration washed with cold acetone dried under reduced pressure The crystals were added to 50 ml of 30% methylamine-methanol the mixture was stirred at room temperature overnight The reaction mixture was concentrated to dryness under reduced pressure the residue was washed with ethanol-ethyl acetate dried under reduced pressure
ソース ID: ord-35842788eadf4ba6b4b7e86ebf2e6951反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To 50 ml of acetone were added 2.46 g of o-anisidine and 3.75 g of benzoyl isothiocyanate, and the mixture is stirred under reflux for 2 hours and, then, allowed to stand overnight in a refrigerator at 5° C. The resulting crystals were collected by filtration, washed with cold acetone and dried under reduced pressure. The crystals were added to 50 ml of 30% methylamine-methanol and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated to dryness under reduced pressure, and the residue was washed with ethanol-ethyl acetate and dried under reduced pressure. The procedure provided 2.08 g of N-(o-methoxyphenyl)thiourea. under reflux for 2 hours The resulting crystals were collected by filtration washed with cold acetone dried under reduced pressure The crystals were added to 50 ml of 30% methylamine-methanol the mixture was stirred at room temperature overnight The reaction mixture was concentrated to dryness under reduced pressure the residue was washed with ethanol-ethyl acetate dried under reduced pressure
ソース ID: ord-de9bab9b5e424189ac8c17363b982488PubChem 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。
