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

Formaldehyde → (2-Methyl-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

HRID 2081497
노트
인쇄 미리보기

반응식

HRID 2081497 반응식
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH:3]([CH2:11][OH:12])[NH:2]1.C=O.[Na].[C:16](=O)([O-])[O-].[K+].[K+]>C(O)=O>[CH3:16][N:2]1[CH:3]([CH2:11][OH:12])[CH2:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH2:1]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 712FormaldehydeHCID 11430Potassium CarbonateHCID 3752277(1,2,3,4-Tetrahydro-isoquinolin-3-yl)-methanolHCID 5360545Sodium

생성물 1

HCID 589740(2-Methyl-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

시약·촉매·용매 1

HCID 284Formic Acid용매

반응 조건

온도
140 °C

실험 절차

In a sealed tube, a mixture of 1.80 g of 1,2,3,4-tetrahydro-3-isoquinolinemethanol, 1.69 g of 90% formic acid and 1.04 g of 35% formalin was heated at 140° C. for 16 hours. The reaction solution was cooled and then made alkaline by addition of 10% aqueous sodium solution. Subsequently, potassium carbonate was added to the solution and a precipitated oil was extracted with chloroform. The extract was dried over anhydrous sodium sulfate and placed under reduced pressure to remove the solvent. There was obtained 1.95 g of 2-methyl-1,2,3,4-tetrahydro-3-isoquinolinemethanol.

후처리

  1. temperatureThe reaction solution was cooled
  2. extractiona precipitated oil was extracted with chloroform
  3. dry with materialThe extract was dried over anhydrous sodium sulfate
  4. customto remove the solvent

출처 및 근거

ORD 기록
ord-5a05dda084ce464681427f416f392cdf
출처 데이터셋
uspto-grants-1993_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05183811

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트