C₂₄H₂₄O₃

Base Information

Chemical Name:C₂₄H₂₄O₃
CAS No.:1327267-95-7
Molecular Formula:C₂₄H₂₄O₃
Molecular Weight:360.453
Hs Code.:

C<sub>24</sub>H<sub>24</sub>O<sub>3</sub>

Synonyms:

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

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Chemical Property of C₂₄H₂₄O₃

Chemical Property:

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Technology Process of C₂₄H₂₄O₃

There total 7 articles about C₂₄H₂₄O₃ 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: 78.0%

: 1327267-88-8
C₂₄H₂₂O₃

: 1327267-95-7
C₂₄H₂₄O₃

Guidance literature:: With palladium 10% on activated carbon; hydrogen; ethylenediamine; In ethyl acetate;
DOI:10.1055/s-0030-1260564

Reference yield:

: 1327268-12-1
(2-{[(4-methoxybenzyl)oxy]methyl}phenyl)methanol

: 1327267-95-7
C₂₄H₂₄O₃

Guidance literature:: Multi-step reaction with 5 steps

1: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 °C

2: sodium hydride / tetrahydrofuran / 16 h / 20 °C

3: sodium tetrahydroborate / tetrahydrofuran; ethanol / 0.17 h / 60 °C

4: acetic acid / water / 16 h

5: palladium 10% on activated carbon; hydrogen; ethylenediamine / ethyl acetate

With sodium tetrahydroborate; oxalyl dichloride; palladium 10% on activated carbon; hydrogen; sodium hydride; acetic acid; dimethyl sulfoxide; ethylenediamine; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; water; ethyl acetate; 1: Swern oxidation / 2: Claisen Schmidt condensation;
DOI:10.1055/s-0030-1260564

Reference yield:

: 87-41-2
2-benzofuran-1(3H)-one

: 1327267-95-7
C₂₄H₂₄O₃

Guidance literature:: Multi-step reaction with 7 steps

1: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 20 °C

2: sodium hydride; sodium iodide / N,N-dimethyl-formamide

3: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 °C

4: sodium hydride / tetrahydrofuran / 16 h / 20 °C

5: sodium tetrahydroborate / tetrahydrofuran; ethanol / 0.17 h / 60 °C

6: acetic acid / water / 16 h

7: palladium 10% on activated carbon; hydrogen; ethylenediamine / ethyl acetate

With sodium tetrahydroborate; lithium aluminium tetrahydride; oxalyl dichloride; palladium 10% on activated carbon; hydrogen; sodium hydride; acetic acid; dimethyl sulfoxide; ethylenediamine; triethylamine; sodium iodide; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; 3: Swern oxidation / 4: Claisen Schmidt condensation;
DOI:10.1055/s-0030-1260564