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Reaction with POCI

Apparently because of these side reactions, 2,4-dihydroxy-5,6,7-trimeth-ylpyrido[2,3-J]pyrimidine (46) on reaction with excess POCI, followed... [Pg.128]

A mixture of 61.7 g POCI, and 54.3 g N-methylformanilide was heated on the steam bath for 15 min which produced a deep red color. This was added to 54.3 g of 5-methoxy-1,2,3,4-tetrahydronaphthalene, and the mixture was heated on the steam bath for 2 h. The reaction mixture was quenched in 1.2 L H20 with very good stirring. The oils generated quickly turned to brown granular solids, which were... [Pg.41]

POCIS extracts and water samples were analyzed for the pharmaceuticals of interest as listed in Table 10.1. Standards and extracts were analyzed on a Quattro Micro triple quadrapole with a Waters 2695 high-pressnre liqnid chromatography (HPLC) and autosampler. Electrospray ionization in positive ion mode was used for detection of target compoimds by multiple reaction monitoring (MRM) with argon collision gas. A Thermo (Bellefonte, PA) Betabasic-18 column (250 x 2.1 mm, 5 p.m, 50°C) was used for separation at a flow rate of 0.2 ml/min with a gradient of methanol... [Pg.193]


See other pages where Reaction with POCI is mentioned: [Pg.65]    [Pg.129]    [Pg.487]    [Pg.336]    [Pg.366]    [Pg.6]    [Pg.104]    [Pg.26]    [Pg.84]    [Pg.111]    [Pg.286]    [Pg.440]    [Pg.561]   
See also in sourсe #XX -- [ Pg.3 , Pg.493 ]




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