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(E)-methyl 3-[4-(dimethylamino)but-1-enyl]-4-(2-iodobenzyloxy)phenylacetate

Base Information
  • Chemical Name:(E)-methyl 3-[4-(dimethylamino)but-1-enyl]-4-(2-iodobenzyloxy)phenylacetate
  • CAS No.:875050-51-4
  • Molecular Formula:C22H26INO3
  • Molecular Weight:479.358
  • Hs Code.:
(E)-methyl 3-[4-(dimethylamino)but-1-enyl]-4-(2-iodobenzyloxy)phenylacetate

Synonyms:(E)-methyl 3-[4-(dimethylamino)but-1-enyl]-4-(2-iodobenzyloxy)phenylacetate

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Chemical Property of (E)-methyl 3-[4-(dimethylamino)but-1-enyl]-4-(2-iodobenzyloxy)phenylacetate
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Technology Process of (E)-methyl 3-[4-(dimethylamino)but-1-enyl]-4-(2-iodobenzyloxy)phenylacetate

There total 7 articles about (E)-methyl 3-[4-(dimethylamino)but-1-enyl]-4-(2-iodobenzyloxy)phenylacetate 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:
[3-(dimethylamino)propyl]triphenylphosphonium iodide; With lithium hexamethyldisilazane; In tetrahydrofuran; toluene; at 20 ℃; for 1h;
methyl [3-formyl-4-(2-iodobenzyloxy)phenyl]acetate; In tetrahydrofuran; toluene; at 20 ℃; for 2.5h;
With hydrogenchloride; potassium carbonate; more than 3 stages;
Guidance literature:
[3-(dimethylamino)propyl]triphenylphosphonium iodide; With lithium hexamethyldisilazane; In tetrahydrofuran; toluene; at 20 - 25 ℃; for 1h;
methyl [3-formyl-4-(2-iodobenzyloxy)phenyl]acetate; In tetrahydrofuran; toluene; at 20 ℃; for 2h;
Guidance literature:
(3-dimethylaminopropyl)-triphenylphosphoniumbromide; With potassium hexamethylsilazane; In toluene; at 20 ℃; for 1h;
methyl [3-formyl-4-(2-iodobenzyloxy)phenyl]acetate; In toluene; at 20 ℃; for 2.5h; optical yield given as %de; stereoselective reaction;
DOI:10.1021/jo300925c
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