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

Nitrogen → 3,N,N-trimethyl-4-(2-triphenylsilanylsulfanyl-ethyl)-benzamide

HRID 1754904
노트
인쇄 미리보기

반응식

HRID 1754904 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[CH:13]=[CH2:14])[C:5]([N:7]([CH3:9])[CH3:8])=[O:6].[C:15]1([Si:21]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[SH:22])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.CC(N=NC(C#N)(C)C)(C#N)C.N#N>C1(C)C=CC=CC=1>[CH3:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[CH2:13][CH2:14][S:22][Si:21]([C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1)([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)[C:5]([N:7]([CH3:9])[CH3:8])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 947NitrogenHCID 6547AzobisisobutyronitrileHCID 621128TriphenylsilanethiolHCID 668162113,N,N-Trimethyl-4-vinylbenzamide

생성물 1

HCID 866727583,N,N-trimethyl-4-(2-triphenylsilanylsulfanyl-ethyl)-benzamide수율 69%

시약·촉매·용매 1

HCID 1140
Toluene
용매

실험 절차

A mixture of 3,N,N-trimethyl-4-vinyl-benzamide (706 mg, 3.73 mmol), triphenylsilanethiol (1.76 g, 6.00 mmol) and AIBN (185 mg, 1.13 mmol) in toluene (16 ml) was heated with stirring at 88° C. for two hours in a sealed test tube in an N2 atmosphere. The reaction mixture was cooled to room temperature and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1) to give 3,N,N-trimethyl-4-(2-triphenylsilanylsulfanyl-ethyl)-benzamide (1.24 g, 69%).

후처리

  1. temperaturewas heated
  2. concentrationconcentrated under reduced pressure
  3. customThe resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1)

출처 및 근거

ORD 기록
ord-886234ea72eb430e950773cdd21d10f0
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09169254B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트