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methyl N-[2-(3-hydroxyprop-1-yn-1-yl)phenyl]carbamate

Base Information Edit
  • Chemical Name:methyl N-[2-(3-hydroxyprop-1-yn-1-yl)phenyl]carbamate
  • CAS No.:1184039-97-1
  • Molecular Formula:C11H11NO3
  • Molecular Weight:205.213
  • Hs Code.:
  • Mol file:1184039-97-1.mol
methyl N-[2-(3-hydroxyprop-1-yn-1-yl)phenyl]carbamate

Synonyms:methyl N-[2-(3-hydroxyprop-1-yn-1-yl)phenyl]carbamate

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Chemical Property of methyl N-[2-(3-hydroxyprop-1-yn-1-yl)phenyl]carbamate Edit
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Technology Process of methyl N-[2-(3-hydroxyprop-1-yn-1-yl)phenyl]carbamate

There total 2 articles about methyl N-[2-(3-hydroxyprop-1-yn-1-yl)phenyl]carbamate 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 copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine; In tetrahydrofuran; at 40 ℃; for 2h; Inert atmosphere;
DOI:10.1021/jo4022293
Guidance literature:
Multi-step reaction with 2 steps
1: pyridine / dichloromethane / 0 - 20 °C / Inert atmosphere; Sealed tube
2: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / tetrahydrofuran / 20 °C / Inert atmosphere; Sealed tube
With pyridine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In tetrahydrofuran; dichloromethane; 2: |Sonogashira Cross-Coupling;
DOI:10.1021/acs.joc.1c01379
Guidance literature:
With 2,2,2-trifluoroethanol; di-isopropyl azodicarboxylate; N-isopropylidene-N’-2-nitrobenzenesulfonyl hydrazine; water; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃; for 4h; Inert atmosphere; Sealed tube;
DOI:10.1021/acs.joc.1c01379
upstream raw materials:

propargyl alcohol

2-iodophenylamine

Downstream raw materials:

methyl 2-methyl-1H-indole-1-carboxylate

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