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

Chloromethyl Methyl Ether → 4,5,6,7-Tetrahydrothieno(3,2-c)pyridinium chloride

HRID 46673
노트
인쇄 미리보기

반응식

HRID 46673 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][CH2:7][NH2:8].[Cl:9][CH2:10]OC>CN(C)C=O>[ClH:9].[S:1]1[C:2]2[CH2:6][CH2:7][NH:8][CH2:10][C:3]=2[CH:4]=[CH:5]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7864Chloromethyl Methyl Ether2회HCID 116521Thiopheneethanamine

생성물 1

HCID 101763424,5,6,7-Tetrahydrothieno(3,2-c)pyridinium chloride수율 31.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

반응 조건

온도
70 °C

실험 절차

To a solution of 12.7 g (0.1 M) 2-(2-thienyl)ethylamine in 20 ml dimethylformamide heated at 55° C. are added, over 10 minutes, 8.05 g (0.1 M) chloromethylmethylether diluted in 10 ml dimethylformamide. After addition of the chloromethylmethylether, the medium is maintained at 70° C. for 2 hours, and is then cooled to room temperature. The desired product precipitates out and is rinsed with acetone, to give 5.5 g 4,5,6,7-tetrahydro-thieno[3,2-c]-pyridine hydrochloride (M.p=225° C.; Yield: 31%).

후처리

  1. additionare added, over 10 minutes
  2. temperatureis then cooled to room temperature
  3. customThe desired product precipitates out
  4. washis rinsed with acetone

출처 및 근거

ORD 기록
ord-edffa91cfc1e41f8bcba666b2299c805
출처 데이터셋
uspto-grants-1979_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04174448

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트