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

Pyridine → n-Pentyltriflate

HRID 1944513
노트
인쇄 미리보기

반응식

HRID 1944513 반응식
N1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(O)CCCC.[S:13]([O:20]S(C(F)(F)F)(=O)=O)([C:16]([F:19])([F:18])[F:17])(=[O:15])=[O:14]>>[CH2:2]([O:20][S:13]([C:16]([F:19])([F:18])[F:17])(=[O:15])=[O:14])[CH2:3][CH2:4][CH2:5][CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1049PyridineHCID 62761-PentanolHCID 67749Trifluoromethanesulfonic anhydride

생성물 1

HCID 10987782n-Pentyltriflate

실험 절차

To a nitrogen flushed round bottom flask equipped with a stir bar was added pyridine (0.81 mL, 10.0 mmol) and n-pentanol (1.09 mL, 10.0 mmol). The reaction was cooled in an ice bath and triflic anhydride (1.69 mL, 10.0 mmol) was added dropwise. The ice bath was allowed to melt over two hours at which time the entire reaction mixture was filtered over a column of silica gel eluting with dichloromethane. The filtrate was carefully evaporated in vacuo then carried on without further purification(1.11 g, 5.04 mmol).

후처리

  1. customTo a nitrogen flushed round bottom flask equipped with a stir bar
  2. temperatureThe reaction was cooled in an ice bath
  3. customthe entire reaction mixture
  4. filtrationwas filtered over a column of silica gel eluting with dichloromethane
  5. customThe filtrate was carefully evaporated in vacuo
  6. customthen carried on without further purification(1.11 g, 5.04 mmol)

출처 및 근거

ORD 기록
ord-905ce1a5152a4b5a9c957a0b8bbd92f8
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08394828B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트