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1-Butanol → 1-(N,N-diphenylaminomethyl)6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

HRID 27152
ノート
印刷プレビュー

反応式

HRID 27152 の反応式
C(O[CH:4](OCC)[CH2:5][N:6]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)C.[ClH:22].[OH:23][C:24]1[CH:25]=[C:26]([CH:30]=[CH:31][C:32]=1[OH:33])[CH2:27][CH2:28][NH2:29].C(O)CCC>Cl.O>[ClH:22].[C:13]1([N:6]([CH2:5][CH:4]2[C:30]3[C:26](=[CH:25][C:24]([OH:23])=[C:32]([OH:33])[CH:31]=3)[CH2:27][CH2:28][NH:29]2)[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 2631-ButanolHCID 65340Dopamine HydrochlorideHCID 12913315N,N-diphenylaminoacetaldehyde diethyl acetal

生成物 1

HCID 705061331-(N,N-diphenylaminomethyl)6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride収率 35.4%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid触媒
HCID 962
Water
溶媒

実験手順

N,N-diphenylaminoacetaldehyde diethyl acetal (3.5 g) and 3,4-dihydroxyphenethylamine hydrochloride (2.1 g) were added to a mixture of n-butyl alcohol (35 ml), water (5 ml) and conc. hydrochloric acid (2 drops) and then the mixture was refluxed for 6.5 hours in a stream of nitrogen. The reaction mixture was concentrated to dryness and the residue was washed with acetone and collected by filtration to recover the starting material, 3,4-dihydroxyphenethylamine (1.2 g). The filtrate was concentrated to give 1-(N,N-diphenylaminomethyl)6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (1.5 g), oil.

後処理

  1. temperaturethe mixture was refluxed for 6.5 hours in a stream of nitrogen
  2. concentrationThe reaction mixture was concentrated to dryness
  3. washthe residue was washed with acetone
  4. filtrationcollected by filtration
  5. customto recover the starting material, 3,4-dihydroxyphenethylamine (1.2 g)
  6. concentrationThe filtrate was concentrated

出典と根拠

ORDレコード
ord-13077b56401f4019b8f40715adce0645
出典データセット
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04220647

反応ノート

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