1252675-90-3

Basic information

• Product Name: 1-(4-benzoyloxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone
• Synonyms: 1-(4-benzoyloxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone
• CAS NO: 1252675-90-3
• Molecular Weight: 392.408
• Mol File: 1252675-90-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(4-benzoyloxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-benzoyloxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone(1252675-90-3)
• EPA Substance Registry System: 1-(4-benzoyloxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone(1252675-90-3)

Safety Data

• Hazardous Substances Data: 1252675-90-3(Hazardous Substances Data)

Upstream product

• 77891-30-6 1-(4-ethoxy-3-methoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propan-1-one 
• 14385-48-9 2-(2-methoxyphenoxy)-acetophenone 
• 78405-40-0 1-(4-ethoxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanol 
• 99634-01-2 3-hydroxy-2-(2-methoxyphenoxy)-1-phenyl-1-propanone 
• 498-02-2 1-(3-methoxy-4-hydroxyphenyl)ethanone 
• 98-88-4 benzoyl chloride 
• 102834-26-4 4-benzoyloxy-3-methoxy-bromoacetylbenzene 
• 90-05-1 2-methoxy-phenol 

Downstream Products

• 22317-34-6 β-hydroxy-α-(2-methoxyphenoxy)4-hydroxy-3-methoxypropiophenone 
• 7382-59-4 guaiacylglycerol-β-guaiacyl ether 
• 90-05-1 2-methoxy-phenol 
• 7382-68-5 1-(4-hydroxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanol 
• 22317-35-7 1-(4-hydroxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethan-1-one 
• 38768-62-6 methyl (2-methoxyphenoxy) ethanoate 
• 498-02-2 1-(3-methoxy-4-hydroxyphenyl)ethanone 
• 102834-26-4 4-benzoyloxy-3-methoxy-bromoacetylbenzene 

Relevant articles and documents

Hydrogenolysis of β-O-4 lignin model dimers by a ruthenium-xantphos catalyst

Hydrogenolysis reactions of so-called lignin model dimers using a Ru-xantphos catalyst are presented (xantphos = 4,5-bis(diphenylphosphino)-9,9- dimethylxanthene). For example, of some nine models studied, the alcohol, 2-(2-methoxyphenoxy)-1-phenylethanol (1), with 5 mol% Ru(H)2(CO) (PPh3)(xantphos) (18) in toluene-d8 at 135 °C for 20 h under N2, gives in ～95% yield the C-O cleavage hydrogenolysis products, acetophenone (14) and guaiacol (17), and a small amount (1H NMR spectroscopy. The in situ Ru(H)2(CO)(PPh 3)3/xantphos system gives similar findings, confirming a recent report (J. M. Nichols et al., J. Am. Chem. Soc., 2010, 132, 12554). The active catalyst is formulated 'for convenience' as 'Ru(CO)(xantphos)'. The hydrogenolysis mechanism proceeds by initial dehydrogenation to give the ketone 4, which then undergoes hydrogenolysis of the C-O bond to give 14 and 17. Hydrogenolysis of 4 to 14 and 17 also occurs using the Ru catalyst under 1 atm H2; in contrast, use of 3-hydroxy-2-(2-methoxyphenoxy)-1-phenyl-1- propanone (7), for example, where the CH2 of 4 has been changed to CHCH2OH, gives a low yield (≤15%) of hydrogenolysis products. Similarly, the diol substrate, 2-(2-methoxyphenoxy)-1-phenyl-1,3-propanediol (9), gives low yields of hydrogenolysis products. These low yields are due to formation of the catalytically inactive complexes Ru(CO)(xantphos)[C(O)C(OC 6H4OMe)C(Ph)O] (20) and/or Ru(CO)(xantphos)[C(O)CHC(Ph)O] (21), where the organic fragments result from dehydrogenation of CH 2OH moieties in 7 and 9. Trace amounts of Ru(CO)(xantphos)(OC 6H4O), a catecholate complex, are isolated from the reaction of 18 with 1. Improved syntheses of 18 and lignin models are also presented.