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octadecanoic acid, 5,5-difluoro-4-oxo-2-<<oxy>methyl>heneicosanyl ester

Base Information
  • Chemical Name:octadecanoic acid, 5,5-difluoro-4-oxo-2-<<oxy>methyl>heneicosanyl ester
  • CAS No.:111935-10-5
  • Molecular Formula:C52H85F2O7P
  • Molecular Weight:891.213
  • Hs Code.:
octadecanoic acid, 5,5-difluoro-4-oxo-2-<<<diphenoxyphosphinyl>oxy>methyl>heneicosanyl ester

Synonyms:octadecanoic acid, 5,5-difluoro-4-oxo-2-<<oxy>methyl>heneicosanyl ester

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Chemical Property of octadecanoic acid, 5,5-difluoro-4-oxo-2-<<oxy>methyl>heneicosanyl ester
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Technology Process of octadecanoic acid, 5,5-difluoro-4-oxo-2-<<oxy>methyl>heneicosanyl ester

There total 13 articles about octadecanoic acid, 5,5-difluoro-4-oxo-2-<<oxy>methyl>heneicosanyl ester 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:
Multi-step reaction with 7 steps
1: 71 percent / pyridine, triphenylphosphine, carbon tetrabromide / CH2Cl2 / 2.5 h
2: 19 percent / tert-butyllithium / diethyl ether
3: 77 percent / 1N HCl / tetrahydrofuran / Ambient temperature
4: 86 percent / pyridine / CHCl3 / 0 deg C up to RT
5: 60 percent / NaBH4 / ethanol; CHCl3 / 0.5 h / 32 °C
6: 87 percent / pyridine / Ambient temperature
7: 60 percent / Jones' reagent / acetone / 3.5 h / Ambient temperature
With pyridine; hydrogenchloride; sodium tetrahydroborate; jones' reagent; carbon tetrabromide; tert.-butyl lithium; triphenylphosphine; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; chloroform; acetone;
DOI:10.1021/ja00260a020
Guidance literature:
Multi-step reaction with 9 steps
1: 72 percent / 4 h / Heating
2: 82 percent / LiAlH4
3: 71 percent / pyridine, triphenylphosphine, carbon tetrabromide / CH2Cl2 / 2.5 h
4: 19 percent / tert-butyllithium / diethyl ether
5: 77 percent / 1N HCl / tetrahydrofuran / Ambient temperature
6: 86 percent / pyridine / CHCl3 / 0 deg C up to RT
7: 60 percent / NaBH4 / ethanol; CHCl3 / 0.5 h / 32 °C
8: 87 percent / pyridine / Ambient temperature
9: 60 percent / Jones' reagent / acetone / 3.5 h / Ambient temperature
With pyridine; hydrogenchloride; sodium tetrahydroborate; lithium aluminium tetrahydride; jones' reagent; carbon tetrabromide; tert.-butyl lithium; triphenylphosphine; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; chloroform; acetone;
DOI:10.1021/ja00260a020
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