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

p-Chlorothiophenol → 2-(((4-Chlorophenyl)thio)methyl)pyridine, hydrochloride

HRID 2286219
노트
인쇄 미리보기

반응식

HRID 2286219 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([SH:8])=[CH:4][CH:3]=1.[OH-].[Na+].Cl.[N:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH2:18]Cl>C(O)C>[ClH:1].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:18][C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][N:12]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7815p-ChlorothiophenolHCID 14798Sodium HydroxideHCID 23392Picolyl chloride hydrochloride

생성물 1

HCID 129532882-(((4-Chlorophenyl)thio)methyl)pyridine, hydrochloride수율 170%

시약·촉매·용매 1

HCID 702Ethanol용매3회

실험 절차

4-Chlorobenzenethiol (5 g) in warm ethanol (5 ml) was added to a solution of sodium hydroxide (2.8 g) in ethanol (50 ml). To the solution was added a solution of 2-picolyl chloride, hydrochloride (5.7 g) in ethanol (25 ml) and the mixture was stirred at ambient temperature for 6 hours. The mixture was filtered and evaporated and the residue was converted into the hydrochloride with ethereal HCl solution and this was recrystallised from ethanol-ether to give 2-(((4-chlorophenyl)thio)methyl)pyridine, hydrochloride (8 g) mp 196°-8° C. (Found: C,52.95; H,4.1; N,5.15 C12H10ClNS.HCl requires C,53.1; H,4.2; N,4.9%).

후처리

  1. filtrationThe mixture was filtered
  2. customevaporated
  3. customthis was recrystallised from ethanol-ether

출처 및 근거

ORD 기록
ord-34c8cd5f9b2543ae8a9f4d10cab205d8
출처 데이터셋
uspto-grants-1982_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04327102

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트