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Methylamine → 1-(m-methoxyphenyl)-N-methyl-2-cyclohexene-1-ethylamine

HRID 1156553
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HRID 1156553 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2([CH2:15][CH:16]=O)[CH2:14][CH2:13][CH2:12][CH:11]=[CH:10]2)[CH:6]=[CH:7][CH:8]=1.[CH3:18][NH2:19]>CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2([CH2:15][CH2:16][NH:19][CH3:18])[CH2:14][CH2:13][CH2:12][CH:11]=[CH:10]2)[CH:6]=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329MethylamineHCID 204600121-(m-Methoxyphenyl)-2-cyclohexene-1-acetaldehyde

생성물 1

HCID 133240571-(m-methoxyphenyl)-N-methyl-2-cyclohexene-1-ethylamine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1.0 g of 1-(m-methoxyphenyl)-2-cyclohexene-1-acetaldehyde is dissolved in 10 ml of methanol, and after treatment with 10 ml of methylamine, the mixture is stirred at room temperature overnight with a magnetic stirrer in a bomb tube. After evaporation of the solvent, the residue is dissolved in ethanol. Then, the solution is treated with 0.5 g of sodium borohydride, stirred at room temperature for 2 hours. The solvent is removed by evaporation, and the residue is taken up with 3 N hydrochloric acid. The aqueous phase is extracted with ether and made alkaline by the addition of concentrated ammonia, whereupon the resulting rac. 1-(m-methoxyphenyl)-N-methyl-2-cyclohexene-1-ethylamine is taken up in methylene chloride. The hydrochloride of this compound melts at 177°-179° C.

후처리

  1. customAfter evaporation of the solvent
  2. dissolutionthe residue is dissolved in ethanol
  3. additionThen, the solution is treated with 0.5 g of sodium borohydride
  4. customThe solvent is removed by evaporation
  5. extractionThe aqueous phase is extracted with ether
  6. additionby the addition of concentrated ammonia

출처 및 근거

ORD 기록
ord-f36e38e5a744450797fc9412da1a38f5
출처 데이터셋
uspto-grants-1982_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04336268

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