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(3-Methoxy-2-propylbenzyl)-dimethylamine → 3-Dimethylaminomethyl-2-propylphenol hydrobromide

HRID 1243741
ノート
印刷プレビュー

反応式

HRID 1243741 の反応式
C[O:2][C:3]1[C:4]([CH2:13][CH2:14][CH3:15])=[C:5]([CH:10]=[CH:11][CH:12]=1)[CH2:6][N:7]([CH3:9])[CH3:8].[BrH:16].C(O)(=O)C>>[BrH:16].[CH3:9][N:7]([CH2:6][C:5]1[C:4]([CH2:13][CH2:14][CH3:15])=[C:3]([OH:2])[CH:12]=[CH:11][CH:10]=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

3

反応物 2

HCID 13780988(3-Methoxy-2-propylbenzyl)-dimethylamineHCID 21893785Acetic Acid Mixture with Hydrobromic Acid

生成物 1

HCID 137809963-Dimethylaminomethyl-2-propylphenol hydrobromide収率 79%

実験手順

(3-Methoxy-2-propylbenzyl)-dimethylamine (1.51 g, 7.28 mmol) was suspended in 30% hydrogen bromide/acetic acid (10 mL) and heated to reflux with stirring for 20 h. The cooled reaction mixture was triturated and decanted with successive portions of diethyl ether (4×), then triturated with diethyl ether overnight. The solid was collected by filtration, washed with ether and dried to give 3-dimethylaminomethyl-2-propylphenol hydrobromide (1.58 g, 79%) as a tan solid.

後処理

  1. temperatureheated
  2. temperatureto reflux
  3. customThe cooled reaction mixture
  4. customwas triturated
  5. customdecanted with successive portions of diethyl ether (4×)
  6. customtriturated with diethyl ether overnight
  7. filtrationThe solid was collected by filtration
  8. washwashed with ether
  9. customdried

出典と根拠

ORDレコード
ord-0d750c46383e46e4bc504d0d5f7b111f
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07119122B2

反応ノート

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