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

N-Iodosuccinimide → Tert-butyl 2-iodothiophen-3-ylcarbamate

HRID 1994165
노트
인쇄 미리보기

반응식

HRID 1994165 반응식
[C:1]([O:5][C:6]([NH:8][C:9]1[CH:13]=[CH:12][S:11][CH:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[I:14]N1C(=O)CCC1=O>C(Cl)Cl>[C:1]([O:5][C:6]([NH:8][C:9]1[CH:13]=[CH:12][S:11][C:10]=1[I:14])=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 736476tert-butyl N-(thiophen-3-yl)carbamate

생성물 1

HCID 11034707Tert-butyl 2-iodothiophen-3-ylcarbamate수율 92.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

In a manner analogous to Campaigne, E. and Monroe, P. A. J.A.C.S., 76, 2447-2450 (1954), to a boiling solution of (tert-butoxy)-N-(3-thiophenyl)carboxamide (21.0 g, 0.1 mol) in methylene chloride (400 mL) add N-iodosuccinimide (23.7 g, 0.1 mol) in small portions. Set the heating bath to 65° C. for 20 min. Take the reaction to room temperature, evaporate the solvent and purify the crude by flash chromatography (Silica gel-Hexane/EtOAc 9:1) to obtain 30.0 g (88%) of (tert-Butoxy)-N-(2-iodo(3-thiophenyl))carboxamide as a white solid.

후처리

  1. customto 65° C.
  2. customfor 20 min
  3. customthe reaction to room temperature
  4. customevaporate the solvent
  5. custompurify the crude by flash chromatography (Silica gel-Hexane/EtOAc 9:1)

출처 및 근거

ORD 기록
ord-61ce1f24e4ce404899ded77a468ac85a
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07652064B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트