홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

N,N'-Dimethylethylenediamine → 3-(2-Hydroxyethyl)-1,4-dimethyl-2-piperazinone

HRID 462503
노트
인쇄 미리보기

반응식

HRID 462503 반응식
[CH3:1][NH:2][CH2:3][CH2:4][NH:5][CH3:6].Br[CH:8]1[CH2:13][CH2:12][O:11][C:9]1=[O:10].C(N(CC)CC)C>O1CCCC1>[OH:11][CH2:12][CH2:13][CH:8]1[N:5]([CH3:6])[CH2:4][CH2:3][N:2]([CH3:1])[C:9]1=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8070N,N'-DimethylethylenediamineHCID 8471TriethylamineHCID 954632(3H)-Furanone, 3-bromodihydro-

생성물 1

HCID 133767393-(2-Hydroxyethyl)-1,4-dimethyl-2-piperazinone

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The mixture of sym. dimethylethylenediamine (1 eq, 53 g), bromobutyrolactone (1 eq, 100 g) and triethylamine (1 eq, 120 ml) in 1000 mL of tetrahydrofuran was refluxed overnight. The crude precipitate was filtered and thoroughly washed with diethyl ether. The ether was evaporated and the residue was purified by elution through a silica gel column using 2% (v/v) methanol in chloroform to obtain the title compound. A small sample was converted into a picrate and crystallized from methanol to obtain the picrate salt of the title compound: mp 157°-159° C.; IR (KBr) 3220, 1650, 1565 and 1330 cm-1 ; UV max (MeOH) 353 nm (ε 18090); and NMR (DMSO-d6) δ 2.1 (m, 2H), 2.9 and 2.93 (singlets, 6H), 3.5 (m, 6H), 3.95 (m, 1H), and 8.55 (s, 2H).

후처리

  1. additionThe mixture of sym
  2. filtrationThe crude precipitate was filtered
  3. washthoroughly washed with diethyl ether
  4. customThe ether was evaporated
  5. customthe residue was purified by elution through a silica gel column

출처 및 근거

ORD 기록
ord-b6b76f1c62444b79be428a68c615f64c
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04515949

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트