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<(2R)-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>propyl>triphenylphoshonium iodide

Base Information
  • Chemical Name:<(2R)-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>propyl>triphenylphoshonium iodide
  • CAS No.:95532-16-4
  • Molecular Formula:C26H30O2P*I
  • Molecular Weight:532.401
  • Hs Code.:
<(2R)-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>propyl>triphenylphoshonium iodide

Synonyms:<(2R)-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>propyl>triphenylphoshonium iodide

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Chemical Property of <(2R)-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>propyl>triphenylphoshonium iodide
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Technology Process of <(2R)-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>propyl>triphenylphoshonium iodide

There total 5 articles about <(2R)-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>propyl>triphenylphoshonium iodide 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 4 steps
1: 98 percent / p-TsOH / Ambient temperature
2: 97 percent / pyridine / 5 h / 0 - 20 °C
3: 85 percent / NaI / acetone / 48 h / Ambient temperature
4: 83 percent / triethyl orthoformate / acetonitrile / 48 h / 75 °C
With pyridine; toluene-4-sulfonic acid; orthoformic acid triethyl ester; sodium iodide; In acetone; acetonitrile;
DOI:10.1021/jo00209a017
Guidance literature:
Multi-step reaction with 3 steps
1: 97 percent / pyridine / 5 h / 0 - 20 °C
2: 85 percent / NaI / acetone / 48 h / Ambient temperature
3: 83 percent / triethyl orthoformate / acetonitrile / 48 h / 75 °C
With pyridine; orthoformic acid triethyl ester; sodium iodide; In acetone; acetonitrile;
DOI:10.1021/jo00209a017
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