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Sodium Iodide → Methyl(2-(piperidin-1-yl)ethyl)amine

HRID 34712
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HRID 34712 반응식
Cl.Cl[CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1.[I-].[Na+].[CH3:13][NH2:14]>CO>[CH3:13][NH:14][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1
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참가 물질

5

반응물 3

HCID 5238Sodium IodideHCID 6329MethylamineHCID 74826Piperidine, 1-(2-chloroethyl)-, hydrochloride

생성물 1

HCID 3157473Methyl(2-(piperidin-1-yl)ethyl)amine수율 73%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 8.0 g of N-(2-chloroethyl)piperidine hydrochloride and 0.5 g of sodium iodide in 60 ml of methanol which contained 40% of methylamine was reacted at 70° C. in a sealed tube for 20 hours. After allowing the reaction mixture to cool down, the reaction mixture was concentrated under reduced pressure. The residue was added with ether, followed by a further addition of 10 g of ground sodium hydroxide. The resulting mixture was stirred for 2 hours. The insoluble material was filtered off and the filtrate was concentrated under the atmospheric pressure. The residue was distilled under reduced pressure to give 4.5 g of a fraction at 80° C./18 Torr (yield: 73%).

후처리

  1. customwas reacted at 70° C. in a sealed tube for 20 hours
  2. temperatureto cool down
  3. concentrationthe reaction mixture was concentrated under reduced pressure
  4. additionThe residue was added with ether
  5. additionfollowed by a further addition of 10 g of ground sodium hydroxide
  6. filtrationThe insoluble material was filtered off
  7. concentrationthe filtrate was concentrated under the atmospheric pressure
  8. distillationThe residue was distilled under reduced pressure
  9. customto give 4.5 g of a fraction at 80° C./18 Torr (yield: 73%)

출처 및 근거

ORD 기록
ord-50a24f73a84448bdaee945495527e333
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04762927

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