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Triethylamine → 1-(3-Chloropropyl)-3-(4-cyanophenyl)urea

HRID 1380201
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HRID 1380201 반응식
C(N(CC)CC)C.Cl.[Cl:9][CH2:10][CH2:11][CH2:12][NH2:13].[C:14]([C:16]1[CH:21]=[CH:20][C:19]([N:22]=[C:23]=[O:24])=[CH:18][CH:17]=1)#[N:15]>C(Cl)Cl>[Cl:9][CH2:10][CH2:11][CH2:12][NH:13][C:23]([NH:22][C:19]1[CH:20]=[CH:21][C:16]([C:14]#[N:15])=[CH:17][CH:18]=1)=[O:24]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 1703804-Cyanophenyl isocyanateHCID 114690951-Propanamine, 3-chloro-, hydrochloride

생성물 1

HCID 136067331-(3-Chloropropyl)-3-(4-cyanophenyl)urea수율 54%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Triethylamine (13.8 g; 137 mmole) was slowly added to a mixture of 3-chloropropylamine hydrochloride (17.8 g; 137 mmole), 4-cyanophenyl isocyanate (19.7 g; 137 mmole), and methylene chloride (200 ml). The resulting solution was stirred until the mild exothermic reaction had subsided and the solvent was removed in vacuo. The product was dissolved in ether, washed with water, dried, and part of the ether removed. The colorless crystals which precipitated out were filtered and dried to give 1-(3-chloropropyl)-3-(4-cyanophenyl)urea (17.5 g; 54% yield). A small portion of the product was recrystallized from water/acetone to give pure product, m.p. 95°-97° C.

후처리

  1. customthe solvent was removed in vacuo
  2. dissolutionThe product was dissolved in ether
  3. washwashed with water
  4. customdried
  5. custompart of the ether removed
  6. customThe colorless crystals which precipitated out
  7. filtrationwere filtered
  8. customdried

출처 및 근거

ORD 기록
ord-d41f1f0f4cf647a08199e8391fa458f1
출처 데이터셋
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04579947

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