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1-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamine → HCID 54499564、化合物

HRID 2206547
ノート
印刷プレビュー

反応式

HRID 2206547 の反応式
[O:1]1[CH2:6][CH2:5][O:4][CH2:3][CH:2]1[CH:7]([NH:9]CC1C=CC(OC)=CC=1)[CH3:8]>CO.[Pd]>[O:1]1[CH2:6][CH2:5][O:4][CH2:3][CH:2]1[CH:7]([NH2:9])[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

4

反応物 1

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

生成物 1

HCID 54499564HCID 54499564、化合物収率 96%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol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. custompurged with hydrogen (30 psi)
  2. filtrationThe reaction mixture was filtered
  3. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-0d0cd262750948fead24ddb2dd3293d9
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09371331B2

反応ノート

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