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

Borane;tetrahydrofuran → HCID 12511634, 화합물

HRID 656297
노트
인쇄 미리보기

반응식

HRID 656297 반응식
[CH3:1][N:2]1[CH:6]=[C:5]([N+:7]([O-:9])=[O:8])[CH:4]=[C:3]1[CH:10]=[O:11].B.O1CCCC1>O1CCCC1>[OH:11][CH2:10][C:3]1[N:2]([CH3:1])[CH:6]=[C:5]([N+:7]([O-:9])=[O:8])[CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723981Borane;tetrahydrofuranHCID 123454411-Methyl-4-nitro-1H-pyrrole-2-carbaldehyde

생성물 1

HCID 12511634HCID 12511634, 화합물수율 90%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
0 °C

실험 절차

Compound 22-1 (550 mg) was dissolved in anhydrous tetrahydrofuran (30 ml) and cooled to 0° C. To the solution was slowly added dropwise 1M borane-tetrahydrofuran (3.25 ml), followed by refluxing at 80° C. for 3 hours. After the completion of the reaction, the solvent was evaporated under reduced pressure to be removed, and then the residue was purified by column-chromatography (ethyl acetate/hexane=2/1) to yield the compound 22-2 (500 mg, 90%).

후처리

  1. temperatureby refluxing at 80° C. for 3 hours
  2. customAfter the completion of the reaction
  3. customthe solvent was evaporated under reduced pressure
  4. customto be removed
  5. customthe residue was purified by column-chromatography (ethyl acetate/hexane=2/1)

출처 및 근거

ORD 기록
ord-3a50af38c0b84081822610b02952bb68
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071650B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트