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

Methanesulfonic Acid → 2-Methyl-6-nitrochroman-4-one

HRID 1722041
노트
인쇄 미리보기

반응식

HRID 1722041 반응식
[N+:1]([C:4]1[CH:16]=[CH:15][C:7]([O:8][CH:9]([CH3:14])[CH2:10][C:11]([OH:13])=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].CS(O)(=O)=O.O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O>>[CH3:14][CH:9]1[CH2:10][C:11](=[O:13])[C:6]2[C:7](=[CH:15][CH:16]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[O:8]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6395Methanesulfonic AcidHCID 14812Phosphorus oxide (P4O10)HCID 147733763-(4-Nitrophenoxy)butyric Acid

생성물 1

HCID 138500312-Methyl-6-nitrochroman-4-one

반응 조건

온도
23 °C

실험 절차

A mixture of 31.2 g (139 mmol) 3-(4-nitrophenoxy)butyric acid, 139 ml methanesulfonic acid and 7 g phosphorus pentoxide was heated on the steam bath for 1.75 hours. The reaction was cooled to 23° C., poured onto 500 ml ice-water mixture and extracted with 2×200 ml diethyl ether. The combined organic extracts were washed with 2×150 ml 1N sodium hydroxide, clarified by filtration, washed with 2×50 ml water and 100 ml brine, dried over magnesium sulfate and concentrated in vacuo to give the crude product as a yellow solid, 2.9 g (10%). Recrystallization from methylene chloride and isopropyl ether gave 1.35 g (4.7%) golden platelets, m.p. 144°-145° C.

후처리

  1. temperaturewas heated on the steam bath for 1.75 hours
  2. extractionextracted with 2×200 ml diethyl ether
  3. washThe combined organic extracts were washed with 2×150 ml 1N sodium hydroxide
  4. filtrationclarified by filtration
  5. washwashed with 2×50 ml water and 100 ml brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-b06f5c113cc8494a80a1532f9623f239
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04853410

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트