C₃₆H₂₅BrO₄

Base Information

Chemical Name:C₃₆H₂₅BrO₄
CAS No.:79970-90-4
Molecular Formula:C₃₆H₂₅BrO₄
Molecular Weight:601.496
Hs Code.:

C<sub>36</sub>H<sub>25</sub>BrO<sub>4</sub>

Synonyms:C₃₆H₂₅BrO₄

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Chemical Property of C₃₆H₂₅BrO₄

Chemical Property:

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Technology Process of C₃₆H₂₅BrO₄

There total 8 articles about C₃₆H₂₅BrO₄ 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:

: 66267-08-1
1,2-dihydrodibenzanthracen-4(3H)-one

: 79970-90-4
C₃₆H₂₅BrO₄

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) hydrazine hydrate, 2.) KOH / 1.) triethylene glycol, 110 deg C, 60 min, 2.) 140 deg C, 2 h

2: 20 percent / benzene; acetic acid / 5 h / 80 °C

3: 99 percent / conc. HCl / acetic acid / 1 h / Heating

4: 66 percent / iodine / tetrahydrofuran; benzene / 3 h / 80 °C

5: N-bromosuccinimid (NBS), 2,2'-azobis(isobutyronitrile) / CCl₄ / 0.67 h / Heating; Irradiation

With potassium hydroxide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); iodine; hydrazine hydrate; hydrogenchloride; In tetrahydrofuran; tetrachloromethane; acetic acid; benzene;
DOI:10.1021/jo00342a041

Reference yield:

: 53-70-3
dibenzo[a,h]anthracene

: 79970-90-4
C₃₆H₂₅BrO₄

Guidance literature:: Multi-step reaction with 6 steps

1: 65 percent / n-pentanol, sodium / 4 h / Heating

2: 61 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) / benzene / 96 h / Ambient temperature

3: 20 percent / benzene; acetic acid / 5 h / 80 °C

4: 99 percent / conc. HCl / acetic acid / 1 h / Heating

5: 66 percent / iodine / tetrahydrofuran; benzene / 3 h / 80 °C

6: N-bromosuccinimid (NBS), 2,2'-azobis(isobutyronitrile) / CCl₄ / 0.67 h / Heating; Irradiation

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); pentan-1-ol; iodine; sodium; 2,3-dicyano-5,6-dichloro-p-benzoquinone; hydrogenchloride; In tetrahydrofuran; tetrachloromethane; acetic acid; benzene;
DOI:10.1021/jo00342a041

Reference yield:

: 153-39-9
1,2,3,4-tetrahydrodibenzanthracene

: 79970-90-4
C₃₆H₂₅BrO₄

Guidance literature:: Multi-step reaction with 4 steps

1: 20 percent / benzene; acetic acid / 5 h / 80 °C

2: 99 percent / conc. HCl / acetic acid / 1 h / Heating

3: 66 percent / iodine / tetrahydrofuran; benzene / 3 h / 80 °C

4: N-bromosuccinimid (NBS), 2,2'-azobis(isobutyronitrile) / CCl₄ / 0.67 h / Heating; Irradiation

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); iodine; hydrogenchloride; In tetrahydrofuran; tetrachloromethane; acetic acid; benzene;
DOI:10.1021/jo00342a041