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

Hydrochloric Acid → 4-[2-Benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)benzylidene]tetrahydropyran

HRID 1766657
노트
인쇄 미리보기

반응식

HRID 1766657 반응식
[Cl-].[CH2:2]([O:9][C:10]1[CH:35]=[CH:34][C:33]([O:36][C:37]2[C:45]([CH3:46])=[CH:44][C:43]([N+:47]([O-:49])=[O:48])=[C:42]3[C:38]=2[CH2:39][CH2:40][CH2:41]3)=[CH:32][C:11]=1[CH2:12][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[H-].[Na+].[O:52]1[CH2:57][CH2:56][C:55](=O)[CH2:54][CH2:53]1.Cl>CS(C)=O>[CH2:2]([O:9][C:10]1[CH:35]=[CH:34][C:33]([O:36][C:37]2[C:45]([CH3:46])=[CH:44][C:43]([N+:47]([O-:49])=[O:48])=[C:42]3[C:38]=2[CH2:39][CH2:40][CH2:41]3)=[CH:32][C:11]=1[CH:12]=[C:55]1[CH2:56][CH2:57][O:52][CH2:53][CH2:54]1)[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 121599Tetrahydro-4H-pyran-4-oneHCID 21110566[2-Benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)benzyl]triphenylphosphonium chloride

생성물 1

HCID 211105754-[2-Benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)benzylidene]tetrahydropyran

시약·촉매·용매 1

HCID 679
Dimethyl Sulfoxide
용매

실험 절차

To a suspension of [2-benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)benzyl]triphenylphosphonium chloride (559 mg) in dimethylsulfoxide (20 mL) was added sodium hydride (60%, 49 mg) at room temperature, the mixture was stirred for 15 min. After adding tetrahydro-4H-pyran-4-one (0.15 mL), the reaction mixture was stirred at room temperature for 6 hours. After adding dropwise diluted hydrochloric acid to make the mixture acidify fully, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed-under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate) to give the title compound (230 mg).

후처리

  1. stirringthe reaction mixture was stirred at room temperature for 6 hours
  2. extractionthe reaction mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThe residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-6043ef445ded4f7badcd4be2cb900cc0
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07230031B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트