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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Cyclopentyloxydibenzo[b,d]furan-1-carbaldehyde → 4-Hydroxy dibenzo[b,d]furan-1-carbaldehyde

HRID 1293435
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인쇄 미리보기

반응식

HRID 1293435 반응식
C1([O:6][C:7]2[C:12]3[O:13][C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=4[C:11]=3[C:10]([CH:20]=[O:21])=[CH:9][CH:8]=2)CCCC1>Br.C(O)(=O)C>[OH:6][C:7]1[C:12]2[O:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[C:11]=2[C:10]([CH:20]=[O:21])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 442251954-Cyclopentyloxydibenzo[b,d]furan-1-carbaldehyde

생성물 1

HCID 442251964-Hydroxy dibenzo[b,d]furan-1-carbaldehyde

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 260Hydrogen Bromide용매

실험 절차

Intermediate 18 was heated in HBr (30-33%) in glacial acetic acid (25 ml) at 50° C. for 7-8 h The reaction contents were poured in ice-water and extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate, and extracted with 10% sodium hydroxide (3×25 ml) solution. The aqueous layer was acidified with conc. HCl to give a white precipitate which was filtered and air dried to obtain the crude product as a white solid (3.2 gm).

후처리

  1. customThe reaction contents
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with saturated sodium bicarbonate
  4. extractionextracted with 10% sodium hydroxide (3×25 ml) solution
  5. customto give a white precipitate which
  6. filtrationwas filtered
  7. customair dried

출처 및 근거

ORD 기록
ord-546a47de5d0845de85c1bfa0f309df12
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07238725B2

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