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

2-Chloroimidazoline sulfate → 2-[4-(4-Isopropoxymethyl-benzyl)-phenyl]-imidazoline

HRID 634795
노트
인쇄 미리보기

반응식

HRID 634795 반응식
[CH:1]([O:4][CH2:5][C:6]1[CH:19]=[CH:18][C:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14](N)=[CH:13][CH:12]=2)=[CH:8][CH:7]=1)([CH3:3])[CH3:2].S(O)(O)(=O)=O.Cl[C:26]1[NH:27][CH2:28][CH2:29][N:30]=1>C(O)(C)C>[CH:1]([O:4][CH2:5][C:6]1[CH:19]=[CH:18][C:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([C:26]3[NH:30][CH2:29][CH2:28][N:27]=3)=[CH:13][CH:12]=2)=[CH:8][CH:7]=1)([CH3:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 125033982-Chloroimidazoline sulfateHCID 218768564-(4-Isopropoxymethylbenzyl)-phenylamine

생성물 1

HCID 218769092-[4-(4-Isopropoxymethyl-benzyl)-phenyl]-imidazoline수율 95.6%

시약·촉매·용매 1

HCID 3776Isopropanol용매

반응 조건

온도
80 °C

실험 절차

To a solution of 4-(4-isopropoxymethylbenzyl)-phenylamine (400 mg, 1.57 mmol) in isopropanol (4.8 mL) at 20° C. under argon atmosphere was added 2-chloro-2-imidazoline sulfate (382 mg, 1.88 mmol). The mixture was heated to 80° C. and stirred for 3 hours. The solvent was evaporated in vacuo, and water and 10% sodium hydroxide was added to pH 11-12. The basic aqueous phase was extracted with dichloromethane (3x 20 mL), and the combined organic layers were washed with water, dried (Na2SO4), and evaporated in vacuo. The crude product was purified by flash chromatography, washed with 0.07M potassium carbonate, and concentrated to give pure 2-[4-(4-isopropoxymethyl-benzyl)-phenyl]-imidazoline (463 mg, 91%) as a clear oil.

후처리

  1. customThe solvent was evaporated in vacuo, and water and 10% sodium hydroxide
  2. additionwas added to pH 11-12
  3. extractionThe basic aqueous phase was extracted with dichloromethane (3x 20 mL)
  4. washthe combined organic layers were washed with water
  5. dry with materialdried (Na2SO4)
  6. customevaporated in vacuo
  7. customThe crude product was purified by flash chromatography
  8. washwashed with 0.07M potassium carbonate
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8b19a98a856c46679d05d8cc0ce8aeb3
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06184242B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트