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

Triphenylphosphine → 3-[2(E)-(Quinolin-2-yl)ethenyl]benzyl chloride

HRID 1198524
노트
인쇄 미리보기

반응식

HRID 1198524 반응식
[Cl:1]N1C(=O)CCC1=O.[N:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][C:10]=1/[CH:19]=[CH:20]/[C:21]1[CH:22]=[C:23]([CH:26]=[CH:27][CH:28]=1)[CH2:24]O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>ClCCl>[N:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][C:10]=1/[CH:19]=[CH:20]/[C:21]1[CH:22]=[C:23]([CH:26]=[CH:27][CH:28]=1)[CH2:24][Cl:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11776TriphenylphosphineHCID 31398ChlorosuccinimideHCID 701100023-[2(E)-(Quinolin-2-yl)ethenyl]benzyl alcohol

생성물 1

HCID 199590993-[2(E)-(Quinolin-2-yl)ethenyl]benzyl chloride

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Solid N-chlorosuccinimide (0.76 g, 5.72 mmol) was added in portions over 5 minutes to a stirred solution of 3-[2(E)-(quinolin-2-yl)ethenyl]benzyl alcohol (1.14 g, 4.58 mmol) and triphenylphosphine (1.50 g, 5.72 mmol) in dichloromethane (100 ml) at 0°-5° C. The mixture was stirred for a further 2 hours at 0°-5° C. then evaporated and the residue was chromatographed on silica in ethyl acetate-hexane (1:3).

후처리

  1. customthen evaporated
  2. customthe residue was chromatographed on silica in ethyl acetate-hexane (1:3)

출처 및 근거

ORD 기록
ord-5a8169a0c7e54d59b773d558c4f432b4
출처 데이터셋
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05281593

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트