2-(methoxycarbonylamino)-2-(4-methoxyphenyl)acetic Acid

Base Information

• Chemical Name: 2-(methoxycarbonylamino)-2-(4-methoxyphenyl)acetic Acid
• CAS No.: 170119-36-5
• Molecular Formula: C₁₁H₁₃NO₅
• Molecular Weight: 239.228
• DSSTox Substance ID: DTXSID80440041
• Mol file: 170119-36-5.mol

Synonyms:2-(methoxycarbonylamino)-2-(4-methoxyphenyl)acetic Acid;170119-36-5;DTXSID80440041;YIFSOCIPNXPSCP-UHFFFAOYSA-N

Chemical Property of 2-(methoxycarbonylamino)-2-(4-methoxyphenyl)acetic Acid

Chemical Property:

• XLogP3: 1.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 239.07937252
• Heavy Atom Count: 17
• Complexity: 273

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C(C(=O)O)NC(=O)OC

Technology Process of 2-(methoxycarbonylamino)-2-(4-methoxyphenyl)acetic Acid

There total 2 articles about 2-(methoxycarbonylamino)-2-(4-methoxyphenyl)acetic Acid 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: 63.2%

2-(4-methoxyphenyl)glycine (2540-53-6,19789-59-4) + methyl chloroformate (79-22-1) → Methoxycarbonylamino-(4-methoxy-phenyl)-acetic acid (170119-36-5)

Guidance literature:

With sodium hydroxide; for 0.333333h; Ambient temperature;

DOI:10.1016/0223-5234(96)88263-8

Reference yield:

5-(4-methoxyphenyl)imidazolidone-2,4-dione (6617-78-3) → Methoxycarbonylamino-(4-methoxy-phenyl)-acetic acid (170119-36-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 86 percent / 10percent aq. NaOH / 24 h / Heating

2: 63.2 percent / 4N NaOH / 0.33 h / Ambient temperature

With sodium hydroxide;

DOI:10.1016/0223-5234(96)88263-8

Reference yield:

Methoxycarbonylamino-(4-methoxy-phenyl)-acetic acid (170119-36-5) → [1-(4-Methoxy-phenyl)-2-pyrrolidin-1-yl-ethyl]-methyl-amine (170119-32-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) N,N'-carbonyldiimidazole / 1.) DMF, 40-45 deg C, 10 min, 2.) DMF, 20 deg C, 30 min

2: 93.6 percent / LAH / diethyl ether / Heating

With lithium aluminium tetrahydride; 1,1'-carbonyldiimidazole; In diethyl ether;

DOI:10.1016/0223-5234(96)88263-8

upstream raw materials:

2-(4-methoxyphenyl)glycine

methyl chloroformate

5-(4-methoxyphenyl)imidazolidone-2,4-dione

Downstream raw materials:

[1-(4-Methoxy-phenyl)-2-pyrrolidin-1-yl-ethyl]-methyl-amine