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Hydrochloric Acid → 1-(4-Isopropoxyphenyl)methanamine

HRID 704381
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HRID 704381 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

HCID 27609361-(4-Isopropoxyphenyl)methanamine수율 14.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-bd5a31ab8df44bd19f538c852dbaee9e
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04987132

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