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4-Methoxybenzylamine → 1-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamine

HRID 1527033
ノート
印刷プレビュー

反応式

HRID 1527033 の反応式
[O:1]1[CH2:6][CH2:5][O:4][CH2:3][CH:2]1[C:7](=O)[CH3:8].[CH3:10][O:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][NH2:19])=[CH:14][CH:13]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCCl>[O:1]1[CH2:6][CH2:5][O:4][CH2:3][CH:2]1[CH:7]([NH:19][CH2:18][C:15]1[CH:16]=[CH:17][C:12]([O:11][CH3:10])=[CH:13][CH:14]=1)[CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 754524-MethoxybenzylamineHCID 5049666Sodium triacetoxyborohydrideHCID 543451261-(1,4-Dioxan-2-yl)ethan-1-one

生成物 1

HCID 897391601-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamine収率 71%

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

To a solution of 1-(1,4-dioxan-2-yl)ethanone (12 g, 92.2 mmol) in 1,2-dichloroethane (100 mL) was added (4-methoxyphenyl)methanamine (25 g, 184.4 mmol) at room temperature. The mixture was allowed to stir for 3 hours, and then sodium triacetoxyborohydride (39 g, 184.4 mmol) was added. The resulting mixture was allowed to stir for 48 hours at room temperature. The reaction mixture was quenched by adding water, extracted with dichloromethane (100 mL×3). The combined organic phase was dried by anhydrous sodium sulphate, and then filtered. The filtrate was concentrated and purified by column chromatograph on silica gel (elute: dichloromethane/methanol 100:1→50:1→20:1) to give 1-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamine (16.4 g, 71%) as a yellow solid. LCMS (M+H+) m/z: calcd. 251.15. found 251.9. To a solution of 1-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamine (5 g, 19.9 mmol) in anhydrous methanol (100 mL) was added palladium 10% on carbon (240 mg, 2 mmol), then purged with hydrogen (30 psi), the mixture was allowed to stir overnight at room temperature. The reaction mixture was filtered, and the filtrate was concentrated to afford the title compound (2.5 g, 96%) as a brown solid.

後処理

  1. stirringto stir for 48 hours at room temperature
  2. customThe reaction mixture was quenched
  3. additionby adding water
  4. extractionextracted with dichloromethane (100 mL×3)
  5. dry with materialThe combined organic phase was dried by anhydrous sodium sulphate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated
  8. custompurified by column chromatograph on silica gel (elute: dichloromethane/methanol 100:1→50:1→20:1)

出典と根拠

ORDレコード
ord-520438dec66245ba92103da3790d51e0
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09085583B2

反応ノート

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