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Hydrochloric Acid → 1-(4-Isopropoxyphenyl)methanamine

HRID 704381
ノート
印刷プレビュー

反応式

HRID 704381 の反応式
[C:1]([BH3-])#[N:2].[Na+].[CH:5]([O:8][C:9]1[CH:16]=[CH:15][C:12](C=O)=[CH:11][CH:10]=1)([CH3:7])[CH3:6].C([O-])(=O)C.[NH4+].Cl>CO>[CH:5]([O:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:1][NH2:2])=[CH:11][CH:10]=1)([CH3:7])[CH3:6]
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 4

HCID 313Hydrochloric AcidHCID 2500774-IsopropoxybenzaldehydeHCID 517165Ammonium AcetateHCID 5003444Sodium cyanoborohydride

生成物 1

HCID 27609361-(4-Isopropoxyphenyl)methanamine収率 14.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Sodium cyanoborohydride (330 mg) was added to a solution of 770 mg of p-isopropoxybenzaldehyde and 4.0 g of ammonium acetate in 20 ml of methanol, and the mixture was stirred at room temperature for 40 hours. The reaction mixture was adjusted to pH 2 or less by addition of concentrated hydrochloric acid, and then concentrated. The residue was dissolved in water and the solution was washed with ethyl acetate. The aqueous layer was adjusted to pH 11 or more by addition of solid potassium hydroxide, and the product was extracted with ethyl acetate. The ethyl acetate layer was washed with water and saturated aqueous solution of sodium chloride in that order, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 110 mg of p-isopropoxybenzylamine.

後処理

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in water
  3. washthe solution was washed with ethyl acetate
  4. additionThe aqueous layer was adjusted to pH 11 or more by addition of solid potassium hydroxide
  5. extractionthe product was extracted with ethyl acetate
  6. washThe ethyl acetate layer was washed with water and saturated aqueous solution of sodium chloride in that order
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-bd5a31ab8df44bd19f538c852dbaee9e
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04987132

反応ノート

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