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2-Chloroethanol → Biphenol-diethanol

HRID 329346
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HRID 329346 반응식
[C:1]1([OH:14])[C:2]([C:7]2[C:8]([OH:13])=[CH:9][CH:10]=[CH:11][CH:12]=2)=[CH:3][CH:4]=[CH:5][CH:6]=1.[OH-].[Na+].Cl[CH2:18][CH2:19][OH:20].[CH2:21]([OH:23])[CH3:22]>>[C:8]1([OH:13])[C:7]([C:2]2[C:1]([OH:14])=[CH:6][CH:5]=[CH:4][CH:3]=2)=[C:12]([CH2:22][CH2:21][OH:23])[C:11]([CH2:18][CH2:19][OH:20])=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 342-ChloroethanolHCID 702Ethanol2회HCID 14798Sodium HydroxideHCID 15731(1,1'-Biphenyl)-2,2'-diol

생성물 1

HCID 19996287Biphenol-diethanol

실험 절차

To biphenol (0.5 mole) and 200 milliliters of absolute ethanol and sodium hydroxide (1.1 millimole) at 80° C. was added dropwise a solution of 2-chloroethanol (1 mole) in 50 milliliters of absolute ethanol. The mixture was refluxed for 48 hours, and then filtered hot and washed twice with boiling ethanol (100 milliliters). Recrystallization from boiling water provided the precursor product biphenol-diethanol, 80 to 85 percent yield of colorless crystals. The melting point for this product was 210 to 211° C.

후처리

  1. temperatureThe mixture was refluxed for 48 hours
  2. filtrationfiltered hot
  3. washwashed twice with boiling ethanol (100 milliliters)
  4. customRecrystallization

출처 및 근거

ORD 기록
ord-3be03b6fed26496e874c1462685d7a91
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04891293

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