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Benzoic acid,4-[(E)-(2,3,5,6,7,8-hexahydro-5,5,8,8-tetramethyl-1H-benz[f]inden-1-ylidene)methyl]-

Base Information
  • Chemical Name:Benzoic acid,4-[(E)-(2,3,5,6,7,8-hexahydro-5,5,8,8-tetramethyl-1H-benz[f]inden-1-ylidene)methyl]-
  • CAS No.:119435-88-0
  • Molecular Formula:C25H28 O2
  • Molecular Weight:360.496
  • Hs Code.:
Benzoic acid,4-[(E)-(2,3,5,6,7,8-hexahydro-5,5,8,8-tetramethyl-1H-benz[f]inden-1-ylidene)methyl]-

Synonyms:Benzoicacid, 4-[(2,3,5,6,7,8-hexahydro-5,5,8,8-tetramethyl-1H-benz[f]inden-1-ylidene)methyl]-,(E)-; 1H-Benz[f]indene, benzoic acid deriv.; AGN 191347

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Chemical Property of Benzoic acid,4-[(E)-(2,3,5,6,7,8-hexahydro-5,5,8,8-tetramethyl-1H-benz[f]inden-1-ylidene)methyl]-
Chemical Property:
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Technology Process of Benzoic acid,4-[(E)-(2,3,5,6,7,8-hexahydro-5,5,8,8-tetramethyl-1H-benz[f]inden-1-ylidene)methyl]-

There total 10 articles about Benzoic acid,4-[(E)-(2,3,5,6,7,8-hexahydro-5,5,8,8-tetramethyl-1H-benz[f]inden-1-ylidene)methyl]- 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:
With potassium hydroxide; In methanol; at 60 ℃;
DOI:10.1021/jm00125a027
Guidance literature:
Multi-step reaction with 9 steps
1: 1) n-BuLi / 1) ether, hexane, r.t., 30 min, 2) ether, r.t., 5 h
2: 90.9 percent / H2 / 10percent Pd/C / 0.5 h
3: 88.6 percent / aq.NaOH / ethanol
4: 1) SOCl2, DMF, 2) AlCl3 / 1) 0 deg C, 1 h, 2) CH2Cl2, 2 h
5: 59.5 percent / NaBH4 / methanol / 0.5 h / 0 °C
6: PBr3 / diethyl ether; hexane / 1 h / 0 °C
7: 38.9 percent / benzene / Ambient temperature
8: various solvent(s) / 5 h / Heating
9: aq.KOH / methanol / 60 °C
With potassium hydroxide; sodium hydroxide; sodium tetrahydroborate; n-butyllithium; aluminium trichloride; thionyl chloride; hydrogen; phosphorus tribromide; N,N-dimethyl-formamide; palladium on activated charcoal; In methanol; diethyl ether; ethanol; hexane; benzene;
DOI:10.1021/jm00125a027
Guidance literature:
Multi-step reaction with 10 steps
1: 1) t-BuLi / 1) ether, pentane, a) r.t., 30 min, b) reflux, 30 min, 2) r.t., 30 min
2: 1) n-BuLi / 1) ether, hexane, r.t., 30 min, 2) ether, r.t., 5 h
3: 90.9 percent / H2 / 10percent Pd/C / 0.5 h
4: 88.6 percent / aq.NaOH / ethanol
5: 1) SOCl2, DMF, 2) AlCl3 / 1) 0 deg C, 1 h, 2) CH2Cl2, 2 h
6: 59.5 percent / NaBH4 / methanol / 0.5 h / 0 °C
7: PBr3 / diethyl ether; hexane / 1 h / 0 °C
8: 38.9 percent / benzene / Ambient temperature
9: various solvent(s) / 5 h / Heating
10: aq.KOH / methanol / 60 °C
With potassium hydroxide; sodium hydroxide; sodium tetrahydroborate; n-butyllithium; aluminium trichloride; thionyl chloride; hydrogen; tert.-butyl lithium; phosphorus tribromide; N,N-dimethyl-formamide; palladium on activated charcoal; In methanol; diethyl ether; ethanol; hexane; benzene;
DOI:10.1021/jm00125a027
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