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Hydrochloric Acid → 3-{[(4-Methoxyphenyl)methyl]amino}propan-1-ol

HRID 515487
ノート
印刷プレビュー

反応式

HRID 515487 の反応式
[NH2:1][CH2:2][CH2:3][CH2:4][OH:5].[CH3:6][O:7][C:8]1[CH:15]=[CH:14][C:11]([CH:12]=O)=[CH:10][CH:9]=1.[BH4-].[Na+].Cl>CO.C(O)(=O)C>[CH3:6][O:7][C:8]1[CH:15]=[CH:14][C:11]([CH2:12][NH:1][CH2:2][CH2:3][CH2:4][OH:5])=[CH:10][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 90863-Amino-1-propanolHCID 312444-MethoxybenzaldehydeHCID 4311764Sodium borohydride

生成物 1

HCID 51009813-{[(4-Methoxyphenyl)methyl]amino}propan-1-ol収率 42%

試薬・触媒・溶媒 2

HCID 176Acetic Acid触媒
HCID 887
Methanol
溶媒

実験手順

To a solution of 3-amino-propan-1-ol (15.0 g, 200 mmol) in methanol (300 ml) was added para-methoxybenzaldehyde (28.6 g, 210 mmol) and a few drops of acetic acid at room temperature. The mixture was stirred at room temperature for 2 hours and cooled to 0° C. After the addition of sodium borohydride (11.4 g, 300 mmol), the mixture was stirred at room temperature for another 2 hours and acidified with 3N hydrochloric acid. The biphasic mixture was stirred at room temperature for 10 minutes. The organic solvent was evaporated under reduced pressure and the residue was partitioned between water and ethyl acetate. The aqueous phase was washed with ethyl acetate and basified with 6N sodium hydroxide. Extraction with chloroform was performed and the organic phase was dried over sodium sulfate followed by concentration in vacuo to afford 3-(4-methoxy-benzylamino)-propan-1-ol as pale yellow oil (16.4 g, 42%).

後処理

  1. temperaturecooled to 0° C
  2. stirringthe mixture was stirred at room temperature for another 2 hours
  3. stirringThe biphasic mixture was stirred at room temperature for 10 minutes
  4. customThe organic solvent was evaporated under reduced pressure
  5. customthe residue was partitioned between water and ethyl acetate
  6. washThe aqueous phase was washed with ethyl acetate and basified with 6N sodium hydroxide
  7. extractionExtraction with chloroform
  8. dry with materialthe organic phase was dried over sodium sulfate
  9. concentrationfollowed by concentration in vacuo

出典と根拠

ORDレコード
ord-6a886eccc8d344bd925a7d6489568f0f
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09108957B2

反応ノート

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