trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene

Base Information

• Chemical Name: trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene
• CAS No.: 88746-66-1
• Molecular Formula: C₃₄H₂₄O₄
• Molecular Weight: 496.562

Synonyms:trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene

Chemical Property of trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene

Chemical Property:

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Technology Process of trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene

There total 10 articles about trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene 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: 60.0%

silver benzoate (532-31-0) + 9,10-dihydrobenzofluoranthene (88746-65-0) → trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene (88746-66-1)

Guidance literature:

With iodine; In benzene; for 3h; Heating;

DOI:10.1021/jo00180a026

Reference yield:

2-methylfluoranthene (33543-31-6) → trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene (88746-66-1)

Guidance literature:

Multi-step reaction with 10 steps

1: 90 percent / N-bromosuccinimide, benzoyl peroxide / CCl₄ / 1.5 h / Heating; Irradiation

2: 1.85 g / diethyl ether / 8 h

3: 1.) diborane, sodium hydroxide, 2.) H₂O₂ / 1.) THF, room temperature, 12h, 2a.) 5 deg C, 2 h, 2b.) reflux , 8h

4: 82 percent / pyridinium chlorochromate / CH₂Cl₂ / 3 h

5: 62 percent / AgNO₃, NaOH / tetrahydrofuran; H₂O / 2 h / Ambient temperature

6: 1.8 g / oxalyl chloride / CH₂Cl₂ / 3 h / Ambient temperature

7: AlCl₃ / CS₂ / 1.) 0 deg C , 1h, 2.) reflux , 30 min

8: 0.8 g / lithium aluminumhydride / tetrahydrofuran / 1 h / Ambient temperature

9: 72 percent / HCl / acetic acid / 1 h / 90 °C

10: 60 percent / I₂ / benzene / 3 h / Heating

With sodium hydroxide; N-Bromosuccinimide; lithium aluminium tetrahydride; aluminium trichloride; Perbenzoic acid; oxalyl dichloride; dihydrogen peroxide; iodine; silver nitrate; pyridinium chlorochromate; diborane; hydrogenchloride; In tetrahydrofuran; carbon disulfide; tetrachloromethane; diethyl ether; dichloromethane; water; acetic acid; benzene;

DOI:10.1021/jo00180a026

Reference yield:

4-(2-fluoranthenyl)-1-butene (88746-59-2) → trans-11,12-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene (88746-66-1)

Guidance literature:

Multi-step reaction with 8 steps

1: 1.) diborane, sodium hydroxide, 2.) H₂O₂ / 1.) THF, room temperature, 12h, 2a.) 5 deg C, 2 h, 2b.) reflux , 8h

2: 82 percent / pyridinium chlorochromate / CH₂Cl₂ / 3 h

3: 62 percent / AgNO₃, NaOH / tetrahydrofuran; H₂O / 2 h / Ambient temperature

4: 1.8 g / oxalyl chloride / CH₂Cl₂ / 3 h / Ambient temperature

5: AlCl₃ / CS₂ / 1.) 0 deg C , 1h, 2.) reflux , 30 min

6: 0.8 g / lithium aluminumhydride / tetrahydrofuran / 1 h / Ambient temperature

7: 72 percent / HCl / acetic acid / 1 h / 90 °C

8: 60 percent / I₂ / benzene / 3 h / Heating

With sodium hydroxide; lithium aluminium tetrahydride; aluminium trichloride; oxalyl dichloride; dihydrogen peroxide; iodine; silver nitrate; pyridinium chlorochromate; diborane; hydrogenchloride; In tetrahydrofuran; carbon disulfide; dichloromethane; water; acetic acid; benzene;

DOI:10.1021/jo00180a026

upstream raw materials:

silver benzoate

9,10-dihydrobenzofluoranthene

2-methylfluoranthene

4-(2-fluoranthenyl)-1-butene

Downstream raw materials:

9-bromo-11β,12α-bis(benzoyloxy)-9,10,11,12-tetrahydrobenzofluoranthene

trans-11,12-bis(benzoyloxy)-11,12-dihydrobenzofluoranthene

cis-11,12-dihydro-11,12-dihydroxybenzofluoranthene

trans-11,12-dihydro-11,12-dihydroxybenzofluoranthene

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