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

Aluminum(III) Chloride → 1,8-Dimethyl-1,2,3,4-tetrahydroisoquinoline

HRID 2293135
노트
인쇄 미리보기

반응식

HRID 2293135 반응식
Cl.Br[CH2:3][CH2:4][NH:5][CH:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH3:14])[CH3:7].[Cl-].[Al+3].[Cl-].[Cl-]>C1C2C(CCCC2)CCC1>[CH3:7][CH:6]1[C:8]2[C:13](=[CH:12][CH:11]=[CH:10][C:9]=2[CH3:14])[CH2:3][CH2:4][NH:5]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6451240Aluminum(III) ChlorideHCID 21476474HCID 21476474, 화합물

생성물 1

HCID 214765001,8-Dimethyl-1,2,3,4-tetrahydroisoquinoline수율 37.1%

시약·촉매·용매 1

HCID 7044Decalin용매

반응 조건

온도
0 °C

실험 절차

To a mixed solution of 14.7 g of the compound (45.5 mM) prepared in Step 4 above and 100 ml of decaline, was added aluminium chloride and reacted at 140°-150° C. for 1.5 hours, which was cooled to 0° C. The reaction mixture was diluted by pouring into ice water and washed with ethyl ether. The reaction mixture was basified by adding aqueous NaOH solution and the solids produced were filtered. The filtrate was extracted from ethyl ether and the extracts was dried over anhydrous sodium sulfate, concentrated under a reduced pressure, to give 3.16 g of the title compound.

후처리

  1. customreacted at 140°-150° C. for 1.5 hours
  2. additionThe reaction mixture was diluted
  3. washwashed with ethyl ether
  4. additionby adding aqueous NaOH solution
  5. customthe solids produced
  6. filtrationwere filtered
  7. extractionThe filtrate was extracted from ethyl ether
  8. dry with materialthe extracts was dried over anhydrous sodium sulfate
  9. concentrationconcentrated under a reduced pressure

출처 및 근거

ORD 기록
ord-531df4841b654e1e91d04de2aba01087
출처 데이터셋
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05686458

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트