C₃₄H₃₀O₅

Base Information

Chemical Name:C₃₄H₃₀O₅
CAS No.:1610527-65-5
Molecular Formula:C₃₄H₃₀O₅
Molecular Weight:518.609
Hs Code.:

C<sub>34</sub>H<sub>30</sub>O<sub>5</sub>

Synonyms:C₃₄H₃₀O₅

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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 C₃₄H₃₀O₅

Chemical Property:

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Technology Process of C₃₄H₃₀O₅

There total 8 articles about C₃₄H₃₀O₅ 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: 58.0%

: 1610527-66-6
C₃₄H₂₈O₅

: 1610527-65-5
C₃₄H₃₀O₅

: 1610527-75-7
C₃₄H₃₀O₅

Guidance literature:: With 20% palladium hydroxide-activated charcoal; hydrogen; In ethyl acetate; at 0 ℃; for 144h;
DOI:10.1002/anie.201307835

Reference yield:

: 1610527-66-6
C₃₄H₂₈O₅

: 1610527-65-5
C₃₄H₃₀O₅

Guidance literature:: With 20% palladium hydroxide-activated charcoal; hydrogen; In ethyl acetate; at 0 ℃; for 110h;
DOI:10.1002/anie.201307835

Reference yield:

: C₂₆H₂₆O₂

: 1610527-65-5
C₃₄H₃₀O₅

Guidance literature:: Multi-step reaction with 10 steps

1.1: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 2 h / 0 - 20 °C

2.1: sodium dihydrogenphosphate; 2-methyl-but-2-ene; sodium chlorite / tert-butyl alcohol; water / 1.5 h / 0 °C

3.1: sodium hydrogencarbonate; iodine / 14 h / 0 °C / Darkness

4.1: sodium hydroxide / tetrahydrofuran; water / 20 h / 50 °C

4.2: 24 h / 0 °C

5.1: oxalyl dichloride / dichloromethane; dimethyl sulfoxide / 0.5 h / -78 °C

5.2: 0.5 h / -78 - 0 °C

6.1: tetrahydrofuran / 14 h / -40 °C

7.1: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 4 h / 0 - 20 °C

8.1: 1,1,1,3,3,3-hexamethyl-disilazane; n-butyllithium / hexane; tetrahydrofuran / 0.5 h / -78 °C

8.2: 0.5 h / -78 °C

8.3: 2 h / -78 °C

9.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

10.1: 20% palladium hydroxide-activated charcoal; hydrogen / ethyl acetate / 110 h / 0 °C

With sodium chlorite; sodium dihydrogenphosphate; n-butyllithium; 2-methyl-but-2-ene; oxalyl dichloride; 20% palladium hydroxide-activated charcoal; hydrogen; iodine; sodium hydrogencarbonate; Dess-Martin periodane; 1,1,1,3,3,3-hexamethyl-disilazane; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; hexane; dichloromethane; water; dimethyl sulfoxide; ethyl acetate; tert-butyl alcohol; 5.1: |Swern Oxidation / 5.2: |Swern Oxidation / 6.1: |Grignard Reaction / 8.1: |Peterson Olefination;
DOI:10.1002/anie.201307835