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Benzyl Alcohol → Phenol

HRID 2049513
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HRID 2049513 반응식
[Ni:1].C[OH:3].[CH2:4]([OH:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>C1C=CC=CC=1>[C:5]1([OH:3])[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[Ni:1].[CH3:4][OH:11]
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참가 물질

5

반응물 2

HCID 244Benzyl AlcoholHCID 22477019Nickel monomethoxide2회

생성물 2

HCID 996PhenolHCID 22477019Nickel monomethoxide

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

[2,2'-thiobis-(4-t-octyl-phenolato)]-benzyl alcohol Nickel II, NiTBP.C6H5OH was prepared as follows: p [2,2'-thiobis-(4-t-octylphenolato)]-2-propanol nickel II prepared as described in Example 4 (83.9 g) was dissolved in benzene (250 ml) and benzyl alcohol (16.2 g) was then added. The resulting solution was heated and refluxed for 1 hr. The displaced 2-propanol and most of the benzene solvent was then removed by distillation and the remainder by rotary evaporation. The complex[2,2'-thiobis-(4-t-octylphenolato)]benzyl alcohol nickel II was thus obtained as a green solid which softened at 150° C., melted partially at 210° C. and was completely fused at 260° C.

후처리

  1. temperatureThe resulting solution was heated
  2. temperaturerefluxed for 1 hr
  3. customThe displaced 2-propanol and most of the benzene solvent was then removed by distillation
  4. customthe remainder by rotary evaporation

출처 및 근거

ORD 기록
ord-b58532c9e4624da39029dc8838fa7f8d
출처 데이터셋
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04198303

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