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

Hydrochloric Acid → Methanesulfonamide, N-(3-oxospiro(benzofuran-2(3H),1'-cyclopropan)-5-yl)-

HRID 894620
노트
인쇄 미리보기

반응식

HRID 894620 반응식
[NH2:1][C:2]1[CH:13]=[CH:12][C:5]2[O:6][C:7]3([C:10](=[O:11])[C:4]=2[CH:3]=1)[CH2:9][CH2:8]3.[CH3:14][S:15](Cl)(=[O:17])=[O:16].Cl>N1C=CC=CC=1>[CH3:14][S:15]([NH:1][C:2]1[CH:13]=[CH:12][C:5]2[O:6][C:7]3([C:10](=[O:11])[C:4]=2[CH:3]=1)[CH2:9][CH2:8]3)(=[O:17])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 31297Methanesulfonyl chlorideHCID 12925991HCID 12925991, 화합물

생성물 1

HCID 3055476Methanesulfonamide, N-(3-oxospiro(benzofuran-2(3H),1'-cyclopropan)-5-yl)-

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of 5-aminospiro[benzo[b]furan-2(3H),1'-cyclopropane]-3-one (0.519 g.) in pyridine (5 ml.) was added methanesulfonyl chloride (0.28 ml.) under ice-cooling, followed by stirring. The reaction mixture was poured into cooled dilute hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried and concentrated to remove the solvent. The residue was recrystallized from ethanol. By the above procedure there was obtained 5-methylsulfonylaminospiro[benzo[b]furan-2(3H),1'-cyclopropane]-3-one as colorless needles melting at 152°-154° C.

후처리

  1. temperaturecooling
  2. additionThe reaction mixture was poured
  3. extractionextracted with ethyl acetate
  4. washThe extract was washed with water
  5. customdried
  6. concentrationconcentrated
  7. customto remove the solvent
  8. customThe residue was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-41791359b72e4a419fb5814ffd264535
출처 데이터셋
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04284644

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트