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Ethylene Glycol → Ammonia

HRID 414618
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HRID 414618 반응식
[C:1]1([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:6]=[CH:5][C:4]([O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]Cl)=[CH:3][CH:2]=1.C(O)CO.[CH3:25][NH:26][CH3:27]>O>[NH3:26].[C:1]1([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:6]=[CH:5][C:4]([O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:26]([CH3:27])[CH3:25])=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 174Ethylene GlycolHCID 674DimethylamineHCID 21281389HCID 21281389, 화합물

생성물 2

HCID 222AmmoniaHCID 21281219HCID 21281219, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

1-(4-biphenyloxy)-6-chlorohexane (5.0 g) and ethylene glycol saturated with dimethylamine (60 ml), were heated at reflux for 3 hours using a dry ice condenser. The solution was added to water. The resulting mixture was extracted with ethyl acetate, dried with sodium sulfate and evaporated. The crude product was chromatographed on silica gel, eluting with a solution of dichloromethane:methanolic ammonia (95:5), to yield 6-(4-biphenyloxy)-1-dimethylaminohexane, which was converted to the hydrochloride salt, m.p. 163°-165° C.

후처리

  1. temperatureat reflux for 3 hours
  2. extractionThe resulting mixture was extracted with ethyl acetate
  3. dry with materialdried with sodium sulfate
  4. customevaporated
  5. customThe crude product was chromatographed on silica gel
  6. washeluting with a solution of dichloromethane

출처 및 근거

ORD 기록
ord-5aecfdafc84f4ef0a0a5ff61d2bfdac1
출처 데이터셋
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04792570

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