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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethylenediamine → Benzofuran-4-carbonitrile

HRID 2041227
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반응식

HRID 2041227 반응식
Br[C:2]1[C:7]2[CH:8]=[CH:9][O:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Cu][C:12]#[N:13].C(N)CN>CN(C=O)C>[O:10]1[C:6]2=[CH:5][CH:4]=[CH:3][C:2]([C:12]#[N:13])=[C:7]2[CH:8]=[CH:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3301EthylenediamineHCID 151587214-Bromo-1-benzofuranHCID 178418546HCID 178418546, 화합물

생성물 1

HCID 13307980Benzofuran-4-carbonitrile수율 41.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Combine 4-bromo-benzofuran (1.0 g, 5.07 mmol), copper(I) cyanide (0.9 g, 10.2 mmol), anhydrous DMF (16 mL) and reflux for 17 h. Cool the reaction mixture to ambient temperature, treat with 50% (v/v) aqueous ethylenediamine (25 mL). Extract the reaction mixture with diethyl ether (3×15 mL), combine the organic extracts, wash with brine (15 mL) and dry over anhydrous Na2SO4. Evaporate the solvent and purify by chromatography on silica gel eluting with hexane/EtOAc (1:0, 9:1 and 4:1) to obtain the desired intermediate as a colorless oil (0.3 g, 39%).

후처리

  1. extractionExtract the reaction mixture with diethyl ether (3×15 mL)
  2. washwash with brine (15 mL)
  3. dry with materialdry over anhydrous Na2SO4
  4. customEvaporate the solvent
  5. custompurify by chromatography on silica gel eluting with hexane/EtOAc (1:0, 9:1 and 4:1)

출처 및 근거

ORD 기록
ord-fcb45d8d95bf4512afb5c6803698158b
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08580780B2

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