5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester

Base Information

Chemical Name:5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester
CAS No.:105343-75-7
Molecular Formula:C₂₈H₃₂N₂O₄
Molecular Weight:460.573
Hs Code.:

Synonyms:5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester

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Chemical Property of 5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester

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Technology Process of 5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester

There total 8 articles about 5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl 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: 40.0%

: 50687-64-4
benzoic acid 4-hydroxy-4-pentylphenyl ester

: 72790-10-4
5-pentyl-pyrimidine-2-carboxylic acid

: 105343-75-7
5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester

Guidance literature:: With tetrachloromethane; triethylamine; triphenylphosphine; In acetonitrile; at 20 ℃; for 10h; Heating;
DOI:10.1007/BF00478133

Reference yield:

: 629-04-9
1-Bromoheptane

: 105343-75-7
5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 65 percent

2: 48 percent

3: 62 percent / CH₃ONa / ethanol / 8 h / Heating

4: 80 percent / aq. 1N NaOH / 5 h / 20 °C

5: 60 percent / 30percent H₂O₂ / acetic acid / 8 h / 70 °C

6: dimethylformamide / 5 h / 100 °C

7: aq. 2N NaOH / 6 h / Heating

8: 40 percent / triphenylphosphine, triethylamine, CCl₄ / acetonitrile / 10 h / 20 °C / Heating

With tetrachloromethane; sodium hydroxide; dihydrogen peroxide; sodium methylate; triethylamine; triphenylphosphine; In ethanol; acetic acid; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1007/BF00478133

Reference yield:

: 688-82-4
1,1-diethoxyheptane

: 105343-75-7
5-Pentyl-pyrimidine-2-carboxylic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 48 percent

2: 62 percent / CH₃ONa / ethanol / 8 h / Heating

3: 80 percent / aq. 1N NaOH / 5 h / 20 °C

4: 60 percent / 30percent H₂O₂ / acetic acid / 8 h / 70 °C

5: dimethylformamide / 5 h / 100 °C

6: aq. 2N NaOH / 6 h / Heating

7: 40 percent / triphenylphosphine, triethylamine, CCl₄ / acetonitrile / 10 h / 20 °C / Heating

With tetrachloromethane; sodium hydroxide; dihydrogen peroxide; sodium methylate; triethylamine; triphenylphosphine; In ethanol; acetic acid; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1007/BF00478133