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(2-Ethyl-3-methoxybenzyl)dimethylamine → 3-Dimethylaminomethyl-2-ethylphenol hydrobromide

HRID 1178519
ノート
印刷プレビュー

反応式

HRID 1178519 の反応式
[CH2:1]([C:3]1[C:12]([O:13]C)=[CH:11][CH:10]=[CH:9][C:4]=1[CH2:5][N:6]([CH3:8])[CH3:7])[CH3:2].[BrH:15].C(O)(=O)C>>[BrH:15].[CH3:8][N:6]([CH2:5][C:4]1[C:3]([CH2:1][CH3:2])=[C:12]([OH:13])[CH:11]=[CH:10][CH:9]=1)[CH3:7]
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 13780987(2-Ethyl-3-methoxybenzyl)dimethylamineHCID 21893785Acetic Acid Mixture with Hydrobromic Acid

生成物 1

HCID 137809943-Dimethylaminomethyl-2-ethylphenol hydrobromide収率 78%

実験手順

(2-Ethyl-3-methoxybenzyl)dimethylamine (1.30 g, 6.73 mmol) was suspended in 30% hydrogen bromide/acetic acid (10 mL) and heated to reflux with stirring for 21 h. The cooled reaction mixture was triturated and decanted with successive portions of diethyl ether (3×), then triturated with diethyl ether overnight. The solid was collected by filtration, washed with ether and dried to give 3-dimethylaminomethyl-2-ethylphenol hydrobromide (1.37 g, 78%) 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 (3×)
  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-77a9641dde704c4da36cca2d70d48e47
出典データセット
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07276528B2

反応ノート

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