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(R)-(-)-1-<3-(benzyloxy)-5-fluorophenyl>-1-(thiazol-2-yl)propyl methyl 4ther

Base Information
  • Chemical Name:(R)-(-)-1-<3-(benzyloxy)-5-fluorophenyl>-1-(thiazol-2-yl)propyl methyl 4ther
  • CAS No.:153441-19-1
  • Molecular Formula:C20H20FNO2S
  • Molecular Weight:357.449
  • Hs Code.:
(R)-(-)-1-<3-(benzyloxy)-5-fluorophenyl>-1-(thiazol-2-yl)propyl methyl 4ther

Synonyms:(R)-(-)-1-<3-(benzyloxy)-5-fluorophenyl>-1-(thiazol-2-yl)propyl methyl 4ther

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Chemical Property of (R)-(-)-1-<3-(benzyloxy)-5-fluorophenyl>-1-(thiazol-2-yl)propyl methyl 4ther
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Technology Process of (R)-(-)-1-<3-(benzyloxy)-5-fluorophenyl>-1-(thiazol-2-yl)propyl methyl 4ther

There total 4 articles about (R)-(-)-1-<3-(benzyloxy)-5-fluorophenyl>-1-(thiazol-2-yl)propyl methyl 4ther 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 2,3-dicyano-5,6-dichloro-p-benzoquinone; In benzene; for 3h; Yield given; Heating;
DOI:10.1021/jm00027a014
Guidance literature:
Multi-step reaction with 2 steps
1: Na2SO4, NH3(gas) / tetrahydrofuran / Heating
2: 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / benzene / 3 h / Heating
With ammonia; sodium sulfate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; benzene;
DOI:10.1021/jm00027a014
Guidance literature:
Multi-step reaction with 3 steps
1: 86 percent / DMSO, oxalyl chloride / CH2Cl2 / 1.25 h / -60 - 20 °C
2: Na2SO4, NH3(gas) / tetrahydrofuran / Heating
3: 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / benzene / 3 h / Heating
With oxalyl dichloride; ammonia; dimethyl sulfoxide; sodium sulfate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; dichloromethane; benzene;
DOI:10.1021/jm00027a014
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