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

1,3-Dibromopropane → 6-(3-Bromopropoxy)-4-piperidino-2,3-dihydrobenzopyran

HRID 65006
노트
인쇄 미리보기

반응식

HRID 65006 반응식
[OH-].[K+].[OH:3][C:4]1[CH:5]=[CH:6][C:7]2[O:12][CH2:11][CH2:10][CH:9]([N:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)[C:8]=2[CH:19]=1.[Br:20][CH2:21][CH2:22][CH2:23]Br>[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.C(OCC)C>[Br:20][CH2:21][CH2:22][CH2:23][O:3][C:4]1[CH:5]=[CH:6][C:7]2[O:12][CH2:11][CH2:10][CH:9]([N:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)[C:8]=2[CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 80011,3-DibromopropaneHCID 14797Potassium HydroxideHCID 137128486-Hydroxy-4-piperidino-2,3-dihydrobenzopyran

생성물 1

HCID 137128496-(3-Bromopropoxy)-4-piperidino-2,3-dihydrobenzopyran

시약·촉매·용매 2

HCID 70681Tetrabutylammonium Chloride촉매HCID 3283Diethyl Ether
용매
2회

실험 절차

Crushed potassium hydroxide (1.15 g) and tetrabutyl ammonium chloride (0.61 g) are added to a solution of the product obtained in Step 3. (4.8 g) in 1,3-dibromopropane (21 ml). The reaction mixture is stirred under nitrogen at RT for 48 hours, diluted with diethyl ether, washed with water and extracted into 5% aq. HCl. The aqueous solution is washed with ether and made alkaline yielding a yellow oil which is taken up in ether, washed, dried, filtered and evaporated to give the desired product as an oil.

후처리

  1. washwashed with water
  2. extractionextracted into 5% aq. HCl
  3. washThe aqueous solution is washed with ether
  4. customyielding a yellow oil which
  5. washwashed
  6. customdried
  7. filtrationfiltered
  8. customevaporated

출처 및 근거

ORD 기록
ord-2b33460dda6649b780d0bc34f34f3f9e
출처 데이터셋
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04612309

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트