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trans-9,10-bis(benzoyloxy)-9,10-dihydrobenzopyrene

trans-9,10-bis(benzoyloxy)-9,10-dihydrobenzo<a>pyrene

Synonyms:trans-9,10-bis(benzoyloxy)-9,10-dihydrobenzopyrene

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Chemical Property of trans-9,10-bis(benzoyloxy)-9,10-dihydrobenzopyrene Edit
Chemical Property:
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Technology Process of trans-9,10-bis(benzoyloxy)-9,10-dihydrobenzopyrene

There total 7 articles about trans-9,10-bis(benzoyloxy)-9,10-dihydrobenzopyrene 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:
Guidance literature:
Multi-step reaction with 3 steps
1: 62 percent / iodine / benzene / 4 h / Heating
2: N-bromosuccinimid (NBS), benzoyl peroxide / CCl4 / 1.5 h / Heating
3: 1,5-diazabicyclo<4.3.0>non-5-ene (DBN) / tetrahydrofuran / 48 h / 5 °C
With N-Bromosuccinimide; Perbenzoic acid; DBN; iodine; In tetrahydrofuran; tetrachloromethane; benzene;
DOI:10.1021/jo00342a041
Guidance literature:
With DBN; In tetrahydrofuran; at 5 ℃; for 48h; Yield given;
DOI:10.1021/jo00342a041
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: 66 percent Chromat. / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) / benzene / 5 h / Ambient temperature
3: 62 percent / iodine / benzene / 4 h / Heating
4: N-bromosuccinimid (NBS), benzoyl peroxide / CCl4 / 1.5 h / Heating
5: 1,5-diazabicyclo<4.3.0>non-5-ene (DBN) / tetrahydrofuran / 48 h / 5 °C
With potassium hydroxide; N-Bromosuccinimide; Perbenzoic acid; DBN; iodine; hydrazine hydrate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; tetrachloromethane; benzene;
DOI:10.1021/jo00342a041
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