C₂₇H₂₂N₂O₄

Base Information

Chemical Name:C₂₇H₂₂N₂O₄
CAS No.:858935-61-2
Molecular Formula:C₂₇H₂₂N₂O₄
Molecular Weight:438.483
Hs Code.:

C<sub>27</sub>H<sub>22</sub>N<sub>2</sub>O<sub>4</sub>

Synonyms:C₂₇H₂₂N₂O₄

Suppliers and Price of C₂₇H₂₂N₂O₄

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of C₂₇H₂₂N₂O₄

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of C₂₇H₂₂N₂O₄

There total 9 articles about C₂₇H₂₂N₂O₄ 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:

: 1201-93-0
1-phenyl-3-dimethylaminoprop-2-enone

: 858935-61-2
C₂₇H₂₂N₂O₄

Guidance literature:: Multi-step reaction with 6 steps

1.1: Zn / acetic acid / 100 - 110 °C

2.1: 60 percent / LiN(Si(CH₃)3)2

3.1: 100 percent / BF₃*Et₂O / CH₂Cl₂

4.1: 99 percent / H₂ / Pd/C / tetrahydrofuran

5.1: dimethylformamide / 2 h / 170 °C

6.1: benzoyl chloride / 20 °C

6.2: K₂CO₃ / diethyl ether / 0.17 h / Heating

With boron trifluoride diethyl etherate; hydrogen; benzoyl chloride; lithium hexamethyldisilazane; zinc; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetic acid; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570420405

Reference yield:

: 858935-65-6
methyl 4-benzoyl-3-methylpyrrole-2-carboxylate

: 858935-61-2
C₂₇H₂₂N₂O₄

Guidance literature:: Multi-step reaction with 5 steps

1.1: 60 percent / LiN(Si(CH₃)3)2

2.1: 100 percent / BF₃*Et₂O / CH₂Cl₂

3.1: 99 percent / H₂ / Pd/C / tetrahydrofuran

4.1: dimethylformamide / 2 h / 170 °C

5.1: benzoyl chloride / 20 °C

5.2: K₂CO₃ / diethyl ether / 0.17 h / Heating

With boron trifluoride diethyl etherate; hydrogen; benzoyl chloride; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570420405

Reference yield:

: 858935-69-0
benzyl 4-benzoyl-3-methylpyrrole-2-carboxylate

: 858935-61-2
C₂₇H₂₂N₂O₄

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 percent / BF₃*Et₂O / CH₂Cl₂

2.1: 99 percent / H₂ / Pd/C / tetrahydrofuran

3.1: dimethylformamide / 2 h / 170 °C

4.1: benzoyl chloride / 20 °C

4.2: K₂CO₃ / diethyl ether / 0.17 h / Heating

With boron trifluoride diethyl etherate; hydrogen; benzoyl chloride; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570420405