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

Dimethylformamide → 3-Chloropyrazine-2-carbonitrile

HRID 325603
노트
인쇄 미리보기

반응식

HRID 325603 반응식
CN(C)C=O.[C:6]([C:8]1[CH:13]=[N:12][CH:11]=[CH:10][N:9]=1)#[N:7].S(Cl)([Cl:17])(=O)=O>C1C=CC=CC=1>[Cl:17][C:13]1[C:8]([C:6]#[N:7])=[N:9][CH:10]=[CH:11][N:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 24648Sulfuryl chlorideHCID 73172Pyrazinecarbonitrile

생성물 1

HCID 2924653-Chloropyrazine-2-carbonitrile수율 65.2%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

In 90 ml of benzene and 9.2 ml of dimethylformamide there was stirred at room temperature cyanopyrazine (12.7 g; 0.12 M) prepared in Step A above, after which there was added over 10 minutes sulfonyl chloride (64.79 g; 0.48 M). The reaction mixture was stirred for 30 minutes in an ice bath, then allowed to warm up to room temperature gradually, after which it was stirred for 5 hours. The benzene layer was decanted, and the reddish oil residue was extracted three times with ether, after which the combined benzene and ether layers were quenched with ice water and cooled in an ice bath. The combined layers were then neutralized with solid sodium bicarbonate, then separated, and the aqueous layer was extracted with ether. The combined organic layers were washed once with a small amount of water, dried with sodium sulfate, filtered, and the solvent evaporated to give the title compound (11 g).

후처리

  1. customprepared in Step A above
  2. stirringafter which it was stirred for 5 hours
  3. customThe benzene layer was decanted
  4. extractionthe reddish oil residue was extracted three times with ether
  5. customafter which the combined benzene and ether layers were quenched with ice water
  6. temperaturecooled in an ice bath
  7. customseparated
  8. extractionthe aqueous layer was extracted with ether
  9. washThe combined organic layers were washed once with a small amount of water
  10. dry with materialdried with sodium sulfate
  11. filtrationfiltered
  12. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-733bffbef1bf4c24911690a97d3791a7
출처 데이터셋
uspto-grants-1984_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04442095

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트