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(η3-3,4-dimethoxybenzyl)cobalt tricarbonyl

Base Information
  • Chemical Name:(η3-3,4-dimethoxybenzyl)cobalt tricarbonyl
  • CAS No.:83268-04-6
  • Molecular Formula:C12H11CoO5
  • Molecular Weight:294.21
  • Hs Code.:
(η3-3,4-dimethoxybenzyl)cobalt tricarbonyl

Synonyms:(η3-3,4-dimethoxybenzyl)cobalt tricarbonyl

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Chemical Property of (η3-3,4-dimethoxybenzyl)cobalt tricarbonyl
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Technology Process of (η3-3,4-dimethoxybenzyl)cobalt tricarbonyl

There total 2 articles about (η3-3,4-dimethoxybenzyl)cobalt tricarbonyl which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With Na#Hg; CO; In diethyl ether; byproducts: NaCl; Co2(CO)8 (1 mmol) was allowed to react with excess Na/Hg in Et2O; resulting Na(Co(CO)4) was decanted under CO or Ar into a Schlenk vessel and 1.9 mmol of org. compd. was added at room temp.; stirring for 1-8 h; the resulting orange soln. was filtered from NaCl and the solvent evapd. at 0°C, leaving a dark-red oil; detected by IR;
DOI:10.1021/ja00272a031
Guidance literature:
With Na#Hg; In diethyl ether; byproducts: NaCl, CO; Co2(CO)8 (1 mmol) was allowed to react with excess Na/Hg in Et2O; resulting Na(Co(CO)4) was decanted under CO or Ar into a Schlenk vessel and 1.9 mmol of org. compd. was added at room temp.; stirring for 20 min; the resulting orange soln. was filtered from NaCl and the solvent evapd. at 0°C, leaving a dark-red oil; detected by IR;
DOI:10.1021/ja00272a031
Guidance literature:
With PPh3; In diethyl ether; freshly prepd. Co-compd. (0.2 mmol) was dissolved in Et2O and PPh3 (0.2mmol) was added at 0°C; the orange colour of the soln. turned quickly to yellow; Et2O was drawn off and the resulting product recrystd. from n-hexane;
DOI:10.1021/ja00272a031
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