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Isopropanol → Octane

HRID 2049514
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HRID 2049514 반응식
[Ni:1].CO.[C:4]([CH:8]1[C:15](C(C)(C)C)(O)[CH:14]=[CH:13][C:10]([CH2:11][OH:12])=[CH:9]1)(C)(C)[CH3:5].CC(O)C>C1C=CC=CC=1>[Ni:1].[CH3:11][OH:12].[CH3:5][CH2:4][CH2:8][CH2:9][CH2:10][CH2:13][CH2:14][CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 3776IsopropanolHCID 22477019Nickel monomethoxideHCID 705893803,4-Di-t-butyl-4-hydroxybenzyl alcohol

생성물 2

HCID 356OctaneHCID 22477019Nickel monomethoxide

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

[2,2'-thiobis-(4-t-octylphenolato)]-2-propanol nickel II (83.9 g) prepared as described in Example 4 was dissolved in benzene (250 ml) and 3,4-di-t-butyl-4-hydroxybenzyl alcohol (35.5 g) was added. The temperature of the mixture was raised to reflux and the resulting solution was refluxed for 2.25 hr. Displaced 2-propanol and benzene (150 ml) were then distilled from the reaction mixture. Remaining solvent was removed by rotary evaporation. From the residue the complex [2,2'-thiobis-(4-t-octylphenolato)]-3,4-di-t-butyl-4-hydroxybenzyl alcohol nickel II was obtained by recrystallization from n-octane as a green solid m.p. 253°-255° C.

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후처리

  1. temperatureThe temperature of the mixture was raised
  2. temperatureto reflux
  3. temperaturethe resulting solution was refluxed for 2.25 hr
  4. distillationwere then distilled from the reaction mixture
  5. customRemaining solvent was removed by rotary evaporation

출처 및 근거

ORD 기록
ord-e9ec0fe38c8b486fa01b6538020fda03
출처 데이터셋
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04198303

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