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[1-(4-methoxyphenyl)-prop-2-yn-1-ol]dicobalthexacarbonyl

Base Information
  • Chemical Name:[1-(4-methoxyphenyl)-prop-2-yn-1-ol]dicobalthexacarbonyl
  • CAS No.:610802-73-8
  • Molecular Formula:C16H10Co2O8
  • Molecular Weight:448.237
  • Hs Code.:
[1-(4-methoxyphenyl)-prop-2-yn-1-ol]dicobalthexacarbonyl

Synonyms:[1-(4-methoxyphenyl)-prop-2-yn-1-ol]dicobalthexacarbonyl

Suppliers and Price of [1-(4-methoxyphenyl)-prop-2-yn-1-ol]dicobalthexacarbonyl
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Chemical Property of [1-(4-methoxyphenyl)-prop-2-yn-1-ol]dicobalthexacarbonyl
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Technology Process of [1-(4-methoxyphenyl)-prop-2-yn-1-ol]dicobalthexacarbonyl

There total 1 articles about [1-(4-methoxyphenyl)-prop-2-yn-1-ol]dicobalthexacarbonyl 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:
In diethyl ether; under N2; soln. of alcohol in dry ether added dropwise to soln. of Co2(CO)8 in ether at 20°C, stirred for 3 h; evapd. under reduced pressure, column chromy. (Florisil, petroleum etherand petroleum ether/ether (5/1) and (2/1)); elem. anal.;
DOI:10.1016/S0022-328X(03)00539-4
Guidance literature:
With HBF4*(CH3)2O; In methanol; diethyl ether; (N2); Schlenk technique; soln. of acid added dropwise over 5 min to soln. of Co complex in ether at -20°C; stirred for 1 h; ethereal layer removed; washed (ether, -20°C); ether added at -20°C; MeOH added; stirred (20°C, 0.5 h; dild. with H2O; org. layer washed (H2O); dried (Na2SO4); evapd. (vac.); filtered through Florisil; elem. anal.;
DOI:10.1021/om900448j
Guidance literature:
In diethyl ether; under N2; HBF4*Me2O added to soln. of Co complex in Et2O at -20°C, stirred at -20°C for 1 h, the ether layer removed, residue washed with ether at -20°C, ether evapd., CH2Cl2 and THF added, stirred at 20°C; TLC (silica gel, petroleum ether/ether (7/1));
DOI:10.1016/S0022-328X(03)00539-4
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