benzoyl-5 methyl-2 benzofuranne

Base Information

Chemical Name:benzoyl-5 methyl-2 benzofuranne
CAS No.:70340-02-2
Molecular Formula:C₁₆H₁₂O₂
Molecular Weight:236.27
Hs Code.:

Synonyms:benzoyl-5 methyl-2 benzofuranne

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Chemical Property of benzoyl-5 methyl-2 benzofuranne

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Technology Process of benzoyl-5 methyl-2 benzofuranne

There total 8 articles about benzoyl-5 methyl-2 benzofuranne 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: 89.0%

: 80645-58-5
bromure de acetoxy-2 benzoyl-5 benzyltriphenylphosphonium

: 70340-02-2
benzoyl-5 methyl-2 benzofuranne

Guidance literature:: With sodium tert-pentoxide; In toluene; Heating;
DOI:10.1016/S0040-4020(01)92357-9

Reference yield:

: 617-02-7
2-methylphenyl benzoate

: 70340-02-2
benzoyl-5 methyl-2 benzofuranne

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / Fries method

2: 94 percent / pyridine / 2 h / 110 °C

3: 75 percent Spectr_. / bromine / CCl₄ / 5 h / Heating; Irradiation

4: 94 percent / toluene / 4 h / Heating

5: 89 percent / sodium t-amylate / toluene / Heating

With bromine; sodium tert-pentoxide; In pyridine; tetrachloromethane; toluene;
DOI:10.1016/S0040-4020(01)92357-9

Reference yield:

: 5326-42-1
3-methyl-4-hydroxybenzophenone

: 70340-02-2
benzoyl-5 methyl-2 benzofuranne

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / pyridine / 2 h / 110 °C

2: 75 percent Spectr_. / bromine / CCl₄ / 5 h / Heating; Irradiation

3: 94 percent / toluene / 4 h / Heating

4: 89 percent / sodium t-amylate / toluene / Heating

With bromine; sodium tert-pentoxide; In pyridine; tetrachloromethane; toluene;
DOI:10.1016/S0040-4020(01)92357-9