反応 #4164102
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-5dd6d24f7c0e43d39512d3ad99d11186表示可能な構造データがありません
C1COCCN1C(=O)C(C2=CC=CC=C2)N製品情報
2-amino-1-morpholin-4-yl-2-phenylethanone (CAS 877125-77-4) 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 24701957
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-5dd6d24f7c0e43d39512d3ad99d11186反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-661d9cceb02a4f29a0d6ac7d4ccf3512反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5dd6d24f7c0e43d39512d3ad99d11186反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a stirred suspension of LAH (6.1 mmol) in THF (25 mL) is added dropwise a solution of 2-amino-1-morpholin-4-yl-2-phenylethanone (670 mmol) in THF (5 mL) at 0° C. The reaction mixture is refluxed for 2 hr, and then the reaction is quenched by the addition of Na2SO4-10H2O at 0° C. After stirring at room temperature for 0.5 h, the resulting mixture is filtered through celite, and the filtrate is concentrated in vacuo to give the title compound, which is directly used for the next reaction without further purification. The reaction mixture is refluxed for 2 hr the reaction is quenched by the addition of Na2SO4-10H2O at 0° C the resulting mixture is filtered through celite the filtrate is concentrated in vacuo
ソース ID: ord-b9c16faaa6f04945b531ba909df66c3b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a stirred suspension of LAH (6.1 mmol) in THF (25 mL) is added dropwise a solution of 2-amino-1-morpholin-4-yl-2-phenylethanone (670 mmol) in THF (5 mL) at 0° C. The reaction mixture is refluxed for 2 hr, and then the reaction is quenched by the addition of Na2SO4-10H2O at 0° C. After stirring at room temperature for 0.5 h, the resulting mixture is filtered through celite, and the filtrate is concentrated in vacuo to give the title compound, which is directly used for the next reaction without further purification. The reaction mixture is refluxed for 2 hr the reaction is quenched by the addition of Na2SO4-10H2O at 0° C the resulting mixture is filtered through celite the filtrate is concentrated in vacuo
ソース ID: ord-b9c16faaa6f04945b531ba909df66c3b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of (2-morpholin-4-yl-2-oxo-1-phenylethyl)carbamic acid tert-butyl ester (3.0 mmol) in CH2Cl2 (6.0 mL) is added TFA (2.0 mL) at 0° C. After stirring at room temperature for 24 h, the reaction mixture is basified to pH 8 with sat. aq NaHCO3. The mixture is extracted with CH2Cl2, and then the combined organic extracts are dried over Na2SO4 and concentrated in vacuo to give the title compound; 1H NMR (CDCl3) δ 2.02 (s, 2H), 3.09-3.14 (m, 1H), 3.20-3.25 (m, 1H), 3.34-3.40 (m, 1H), 3.46-3.60 (m, 3H), 3.65-3.71 (m, 1H), 3.74-3.80 (m, 1H), 7.27-7.34 (m, 5H). The mixture is extracted with CH2Cl2 the combined organic extracts are dried over Na2SO4 concentrated in vacuo
ソース ID: ord-4d3c0ccf77004ad2a9b86a0b85094e09反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a stirred suspension of LAH (6.1 mmol) in THF (25 mL) is added dropwise a solution of 2-amino-1-morpholin-4-yl-2-phenylethanone (670 mmol) in THF (5 mL) at 0° C. The reaction mixture is refluxed for 2 hr, and then the reaction is quenched by the addition of Na2SO4-10H2O at 0° C. After stirring at room temperature for 0.5 h, the resulting mixture is filtered through celite, and the filtrate is concentrated in vacuo to give the title compound, which is directly used for the next reaction without further purification. The reaction mixture is refluxed for 2 hr the reaction is quenched by the addition of Na2SO4-10H2O at 0° C the resulting mixture is filtered through celite the filtrate is concentrated in vacuo
ソース ID: ord-b9c16faaa6f04945b531ba909df66c3b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of (2-morpholin-4-yl-2-oxo-1-phenylethyl)carbamic acid tert-butyl ester (3.0 mmol) in CH2Cl2 (6.0 mL) is added TFA (2.0 mL) at 0° C. After stirring at room temperature for 24 h, the reaction mixture is basified to pH 8 with sat. aq NaHCO3. The mixture is extracted with CH2Cl2, and then the combined organic extracts are dried over Na2SO4 and concentrated in vacuo to give the title compound; 1H NMR (CDCl3) δ 2.02 (s, 2H), 3.09-3.14 (m, 1H), 3.20-3.25 (m, 1H), 3.34-3.40 (m, 1H), 3.46-3.60 (m, 3H), 3.65-3.71 (m, 1H), 3.74-3.80 (m, 1H), 7.27-7.34 (m, 5H). The mixture is extracted with CH2Cl2 the combined organic extracts are dried over Na2SO4 concentrated in vacuo
ソース ID: ord-4d3c0ccf77004ad2a9b86a0b85094e09PubChem 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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