{3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl ester
CAS No.:913172-25-5
Molecular Formula:C₁₈H₃₀N₂O₃
Molecular Weight:322.448
Hs Code.:

{3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid <i>tert</i>-butyl ester

Synonyms:{3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl ester

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Chemical Property of {3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl ester

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Technology Process of {3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl ester

There total 5 articles about {3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl 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:

Reference yield: 10.0%

: 913172-20-0
[3-(4-bromoethynyl-phenoxy)-propyl]-carbamic acid tert-butyl ester

: 124-40-3
dimethyl amine

: 913172-25-5
{3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl ester

Guidance literature:: [3-(4-bromoethynyl-phenoxy)-propyl]-carbamic acid tert-butyl ester; dimethyl amine; In tetrahydrofuran; acetonitrile; at 20 ℃;

With sodium tetrahydroborate; In tetrahydrofuran; methanol; acetonitrile; at 0 ℃; for 0.5h;
DOI:10.1021/ol061599w

Reference yield:

: 913172-10-8
tert-butyl 3-(4-iodophenoxy)propylcarbamate

: 913172-25-5
{3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 100 percent / CuI; triethylamine / Pd(PPh₃)4 / 4 h / 20 °C

2.1: 71 percent / AgNO₃; NBS / acetone / 0 - 20 °C

3.1: tetrahydrofuran; acetonitrile / 20 °C

3.2: 10 percent / NaBH₄ / tetrahydrofuran; acetonitrile; methanol / 0.5 h / 0 °C

With N-Bromosuccinimide; copper(l) iodide; silver nitrate; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; acetone; acetonitrile; 1.1: Sonogashira cross-coupling;
DOI:10.1021/ol061599w

Reference yield:

: 540-38-5
p-Iodophenol

: 913172-25-5
{3-[4-(2-dimethylamino-ethyl)-phenoxy]-propyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 percent / Cs₂CO₃; NaI / acetonitrile / 8 h / 65 °C

2.1: 100 percent / CuI; triethylamine / Pd(PPh₃)4 / 4 h / 20 °C

3.1: 71 percent / AgNO₃; NBS / acetone / 0 - 20 °C

4.1: tetrahydrofuran; acetonitrile / 20 °C

4.2: 10 percent / NaBH₄ / tetrahydrofuran; acetonitrile; methanol / 0.5 h / 0 °C

With N-Bromosuccinimide; copper(l) iodide; caesium carbonate; silver nitrate; triethylamine; sodium iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; acetone; acetonitrile; 2.1: Sonogashira cross-coupling;
DOI:10.1021/ol061599w