C₂₆H₃₄O₄

Base Information

Chemical Name:C₂₆H₃₄O₄
CAS No.:106470-13-7
Molecular Formula:C₂₆H₃₄O₄
Molecular Weight:410.554
Hs Code.:

C<sub>26</sub>H<sub>34</sub>O<sub>4</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 C₂₆H₃₄O₄

Chemical Property:

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Technology Process of C₂₆H₃₄O₄

There total 2 articles about C₂₆H₃₄O₄ 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: 100.0%

: 7081-78-9
1-chloroethyl ethyl ether

: 37619-52-6,37619-64-0,81768-39-0,106565-04-2
(1RS,2RS,3RS,5SR)-3,5-bis(phenylmethoxy)-2-(2-propenyl)-1-cyclopentanol

: 106470-13-7,106565-08-6
C₂₆H₃₄O₄

Guidance literature:: With N,N-diethylaniline; In dichloromethane; at 22 ℃; for 22h;
DOI:10.1021/jo00381a027

Reference yield:

: 20476-33-9
1α,4α-dibenzyloxy-2α,3α-epoxycyclopentane

: 106470-13-7,106565-08-6
C₂₆H₃₄O₄

Guidance literature:: Multi-step reaction with 2 steps

1: 98.6 percent / diethyl ether / 1.) -78 deg C, 1.5 h, 2.) from -78 deg C to -30 deg C, 2 h

2: 100 percent / N,N-diethylaniline / CH₂Cl₂ / 22 h / 22 °C

With N,N-diethylaniline; In diethyl ether; dichloromethane;
DOI:10.1021/jo00381a027

Reference yield:

: 106470-13-7,106565-08-6
C₂₆H₃₄O₄

: 106470-40-0
(1SR,3SR,5RS,6RS,7RS)-6-<(methanesulfonyl)oxy>-3-phenyl-7-propyl-2,4-dithiabicyclo<3.2.1>octane

Guidance literature:: Multi-step reaction with 8 steps

1: Na, ethanol / diethyl ether; liquid ammonia / 1 h / -78 °C

2: 100 percent / pyridine / 120 h / 0 °C

3: 100 percent / p-toluenesulfonic acid / methanol / 4 h / 22 °C

4: 92 percent / H₂ / 5percent Pd/C / ethanol; ethyl acetate / 9 h / 22 °C

5: 58 percent / dimethylformamide / 0.6 h / 84 °C

6: 4.6percent methanolic HCl / 4 h / 55 °C

7: BF₃*OEt₂ / CHCl₃ / 1 h / 23 °C

8: 100 percent / triethylamine / CH₂Cl₂ / 0.5 h / 0 °C

With pyridine; hydrogenchloride; ethanol; boron trifluoride diethyl etherate; hydrogen; sodium; toluene-4-sulfonic acid; triethylamine; palladium on activated charcoal; In methanol; diethyl ether; ethanol; dichloromethane; chloroform; ammonia; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jo00381a027