Sodium amide → 3-(5,6,7,8-Tetrahydroquinol-8-yl)propylamine

HRID 1607038

반응식

HRID 1607038 반응식
[N:1]1[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[NH2-].[Na+].Cl.Cl[CH2:15][CH2:16][CH2:17][NH2:18]>N>[N:1]1[C:10]2[CH:9]([CH2:15][CH2:16][CH2:17][NH2:18])[CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1

참가 물질

5

반응물 3

HCID 24533Sodium amideHCID 663355,6,7,8-TetrahydroquinolineHCID 114690951-Propanamine, 3-chloro-, hydrochloride

생성물 1

HCID 198517793-(5,6,7,8-Tetrahydroquinol-8-yl)propylamine수율 26.5%

시약·촉매·용매 1

HCID 222Ammonia용매

실험 절차

5,6,7,8-Tetrahydroquinoline (20 g) was added quickly to sodamide (17.6 g) in liquid ammonia (250 ml) to give a dark red coloured solution. 3-Chloropropylamine hydrochloride (28.9 g) was added in portions over four hours when loss of colour was permanent after which the reaction was stirred for a further 2 hours and then quenched with ammonium chloride (20 g). The liquid ammonia was allowed to evaporate and the residues were partitioned between chloroform and water. The pH was lowered to 6 and the chloroform layer was discarded. The aqueous layer was basified (pH 12-14), and extracted with chloroform, the chloroform extracts were dried, combined, evaporated and the residue was vacuum distilled to give 3-(5,6,7,8-tetrahydroquinol-8-yl)propylamine (7.58 g), b.p. 92°-94° C. at 0.1 mm Hg.

후처리

  1. customto give a dark red coloured solution
  2. customquenched with ammonium chloride (20 g)
  3. customto evaporate
  4. customthe residues were partitioned between chloroform and water
  5. extractionextracted with chloroform
  6. dry with materialthe chloroform extracts were dried
  7. customevaporated
  8. distillationdistilled

출처 및 근거

ORD 기록
ord-df8e7aeb9870434eb52d3e6a27c8d83a
출처 데이터셋
uspto-grants-1989_09
특허 번호
US04863933

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