(+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester

Base Information

• Chemical Name: (+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester
• CAS No.: 869347-33-1
• Molecular Formula: C₂₀H₁₈N₄O₃
• Molecular Weight: 362.388
• Mol file: 869347-33-1.mol

Synonyms:(+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester

Chemical Property of (+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester

There total 4 articles about (+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl 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: 65.0%

(+/-)-α-bromo-(3-azidophenyl)acetic acid ethyl ester (869347-28-4) + 2-(1H-pyrrol-1-yl)phenol (32277-91-1) → (+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester (869347-33-1)

Guidance literature:

2-(1H-pyrrol-1-yl)phenol; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 1h;

(+/-)-α-bromo-(3-azidophenyl)acetic acid ethyl ester; In tetrahydrofuran; for 15h; Heating;

DOI:10.1021/jm050257d

Reference yield:

3-azidophenylacetic acid ethyl ester (869347-25-1) → (+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester (869347-33-1)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 74 percent / N-bromosuccinimide; AIBN / CCl₄ / 5 h / Heating

2.1: NaH / tetrahydrofuran / 1 h / 20 °C

2.2: 65 percent / tetrahydrofuran / 15 h / Heating

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sodium hydride; In tetrahydrofuran; tetrachloromethane;

DOI:10.1021/jm050257d

Reference yield:

3-amino phenylacetic acid (14338-36-4) → (+/-)-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester (869347-33-1)

Guidance literature:

Multi-step reaction with 4 steps

1.1: aq. HCl; H₂SO₄; NaNO₂ / 0.5 h / 0 °C

1.2: 72 percent / aq. NaN₃ / 5 h / 0 °C

2.1: 76 percent / H₂SO₄ / 5 h / Heating

3.1: 74 percent / N-bromosuccinimide; AIBN / CCl₄ / 5 h / Heating

4.1: NaH / tetrahydrofuran / 1 h / 20 °C

4.2: 65 percent / tetrahydrofuran / 15 h / Heating

With hydrogenchloride; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sulfuric acid; sodium hydride; sodium nitrite; In tetrahydrofuran; tetrachloromethane;

DOI:10.1021/jm050257d

upstream raw materials:

(+/-)-α-bromo-(3-azidophenyl)acetic acid ethyl ester

2-(1H-pyrrol-1-yl)phenol

3-azidophenylacetic acid ethyl ester

3-amino phenylacetic acid

Downstream raw materials:

(+/-)-α-ethyl-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid

5-(3-azido-phenyl)-5-ethyl-6-oxa-10b-aza-benzo[e]azulen-4-one

(+/-)-α-ethyl-α-(3-azidophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester