1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic acid

Base Information

Chemical Name:1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic acid
CAS No.:1310817-14-1
Molecular Formula:C₁₄H₁₅NO₄
Molecular Weight:261.277
Hs Code.:

Synonyms:1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic acid

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Chemical Property of 1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic acid

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Technology Process of 1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic acid

There total 6 articles about 1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic 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: 98.0%

: 1310817-10-7
ethyl 1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylate

: 1310817-14-1
1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic acid

Guidance literature:: ethyl 1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylate; With ethanol; sodium hydroxide; at 65 ℃; for 3h;

With sodium hydrogen sulfate;

Reference yield:

: 62577-90-6
4-(cyclopropyloxy)benzoic acid

: 1310817-14-1
1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 0 °C

2: triethylamine / dichloromethane / 16 h / 20 °C

3: ethanol; sodium hydroxide / 3 h / 65 °C

With oxalyl dichloride; ethanol; triethylamine; sodium hydroxide; N,N-dimethyl-formamide; In dichloromethane;

Reference yield:

: 106-41-2
4-bromo-phenol

: 1310817-14-1
1-[[4-(cyclopropoxy)benzoyl]amino]cyclopropanecarboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium carbonate / bis(1,5-cyclooctadiene)diiridium(I) dichloride / toluene / 2.5 h / 100 °C

2.1: diethylzinc / n-heptane; 1,2-dichloro-ethane / 3 h / 0 - 5 °C

3.1: n-butyllithium / tetrahydrofuran; diethyl ether; hexane; ethyl acetate / 0.33 h / -78 - -70 °C

3.2: 0.67 h / -78 °C

4.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 0 °C

5.1: triethylamine / dichloromethane / 16 h / 20 °C

6.1: ethanol; sodium hydroxide / 3 h / 65 °C

With n-butyllithium; oxalyl dichloride; ethanol; diethylzinc; sodium carbonate; triethylamine; sodium hydroxide; bis(1,5-cyclooctadiene)diiridium(I) dichloride; N,N-dimethyl-formamide; In tetrahydrofuran; diethyl ether; hexane; n-heptane; dichloromethane; ethyl acetate; 1,2-dichloro-ethane; toluene;