反応 #4173620
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-da9c15b2bc2e44669d2c31bed5db69a9表示可能な構造データがありません
CC(C)CNC製品情報
N,2-dimethylpropan-1-amine (CAS 625-43-4) 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 12249
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-da9c15b2bc2e44669d2c31bed5db69a9反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9eb1f1c0687243fa9c43b92d28c63c39反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3f4a03955fbe4313997cb193cf6d501a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5cf4010a082d45658e58f6a2b7177509反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-96f4672d80bf4a07a862ad988aff6d2b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-41846ebe005b4af5ad0e1d67014af51d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c4c3d38761a241ae9f40dacd2f946aab反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-0a1e56e1a3c14d1a9b7a00fcc80b43b8反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b355c6d05d7f44a6bbf560d79169d418反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a stirring solution of N-methylisobutylamine (3.21 g, 36.8 mmol, 4.45 mL) in 40 mL of CHCl3 was added benzoyl isothiocyanate (6.0 g, 36.8 mmol, 4.95 mL) After stirring for 45 min, the solution was concentrated to yield the title compound as a pale yellow solid (9.22 g, 100%). 1HNMR (400 MHz, CDCl3; 2:1 mixture of rotamers) δ 7.86 (d, 2H), 7.60 (t, 1H), 7.50 (t, 2H), 3.90 (d, 2H), 3.44 (s, 3H), 3.41 (d, 2H), 3.27 (s, 3H), 2.35-2.32 (m, 1H), 2.13 (m, 1H), 1.06 (d, 6H), 0.90 (d, 6H). the solution was concentrated
ソース ID: ord-479882d720f744f1a83c39b9614a0777反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To an ice-cold, stirred solution of methyl 3-(hydroxymethyl)-5-methylbenzoate (200 mg, 1.1 mmol) in methylene chloride (2.2 mL) is added triethylamine (0.304 mL, 2.2 mmol) followed by methanesulfonyl chloride (0.116 mL, 1.5 mmol). The reaction mixture is stirred for 15 min and filtered. N-Methylisobutylamine (287 mg, 3.3 mmol) is added to the filtrate, and the reaction mixture is stirred at room temperature for 5 h. The reaction mixture is diluted with methylene chloride (10 mL), washed with 1 N hydrochloric acid, and saturated sodium bicarbonate, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 15% ethyl acetate/hexanes) provides the title compound. 1H NMR (300 MHz, CDCl3) δ 7.77 (s, 1H), 7.73 (s, 1H), 7.36 (s, 1H), 3.90 (s, 3H), 3.44 (s, 2H), 2.38 (s, 3H), 2.14 (s, 3H), 2.10 (d, J=8 Hz, 2H), 1.81 (m, 1H), 0.90 (d, J=7 Hz, 6H). filtered the reaction mixture is stirred at room temperature for 5 h washed with 1 N hydrochloric acid, and saturated sodium bicarbonate dried (magnesium sulfate) filtered concentrated under reduced pressure Purification by flash column chromatography (silica, 15% ethyl acetate/hexanes)
ソース ID: ord-3f90a1bfd7a342bc9ea6c2be329943d0反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-da9c15b2bc2e44669d2c31bed5db69a9PubChem 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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