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I acetic acid

Acetylated Castor Oil ----> Drying Oil -i- Acetic Acid Vapour... [Pg.293]

Fig. 4.1. Potential ranges of solvents, (a) h.n.p.s of acids. I, Acetic acid II, benzoic acid III, formic acid IV, salicylic acid V, sulphuric acid VI, p-toluenesulphonic acid, (b) h.n.p.s of conjugate acids of I, n-butylamine II, piperidine III, ethylenediamine (1) IV, ammonia V, ethylenediamine (2) VI, pyridine. Fig. 4.1. Potential ranges of solvents, (a) h.n.p.s of acids. I, Acetic acid II, benzoic acid III, formic acid IV, salicylic acid V, sulphuric acid VI, p-toluenesulphonic acid, (b) h.n.p.s of conjugate acids of I, n-butylamine II, piperidine III, ethylenediamine (1) IV, ammonia V, ethylenediamine (2) VI, pyridine.
Solvent system I Acetic Acid Water (15 85) II Acetic Acid Water (40 60) III Butanol-(l) Acetic Acid Water (4 1 5) upper layer IV Water Butanone(2) MeOH Pentanedione (65 15 15 5)... [Pg.40]

Figure 8 Guest-dependent polymorphism in CA inclusion crystals with (a) acetophenone, (b) y-valerolactone, (c) ethynylbenzene, (d) 2-fluoropropiophenone, (e) m-chloroaniline, (f) water (Form I), (g) water (Form II), (h) 3-methylcyclohexanone, (i) acetic acid, (j) m-fluoroaniline, (k) 1,2,3-trimethylbenzene, and (1) acrylonitrile. Hydrogen atoms are omitted for clarity. Carbon, nitrogen and oxygen atoms are represented by open, gray and tilled circles, respectively. [Pg.99]

Unless otherwise indicated in the monograph, use Method I Acetic Acid-Isooctane Method. [Pg.108]

Fig. 17.12 In situ bridged aza Michael approach in solution and on solid phase to obtain tetrahydroquinoline-based tricyclic compounds, (a) (i) acetic acid/THF/H20, RT (ii) TESOTf, pyridine, CH2CI2, -40°C (iii) Pd(PPh3)4, morpholine, CH2CI2, RT (c) Et3N, benzoyl chloride or cinnamoyl chloride, CH2CI2, O C to RT. Fig. 17.12 In situ bridged aza Michael approach in solution and on solid phase to obtain tetrahydroquinoline-based tricyclic compounds, (a) (i) acetic acid/THF/H20, RT (ii) TESOTf, pyridine, CH2CI2, -40°C (iii) Pd(PPh3)4, morpholine, CH2CI2, RT (c) Et3N, benzoyl chloride or cinnamoyl chloride, CH2CI2, O C to RT.
Di methyl-i-butylsilyl ethers are cleaved by 2 I acetic acid-water at 25° or by treat mcnl with tetra-n-butylammonium fluoride (this volume) in THF at 25°. [Pg.177]

I. Acetic acid molecules react with the water molecules to form a new compound. [Pg.511]

TABLE 15-S Water -i- Acetic Acid + Methyl Isobutyl Ketone Equilibrium Data at 25 C... [Pg.1738]

Adams et al.. As mobile phase, water - methanol - acetonitrile - 10 ml/I acetic acid (788 ... [Pg.392]

See other pages where I acetic acid is mentioned: [Pg.108]    [Pg.10]    [Pg.147]    [Pg.239]    [Pg.82]    [Pg.438]    [Pg.104]    [Pg.146]    [Pg.201]    [Pg.384]    [Pg.548]    [Pg.259]    [Pg.10]    [Pg.1008]    [Pg.188]    [Pg.16]    [Pg.966]    [Pg.1008]    [Pg.872]    [Pg.384]    [Pg.449]    [Pg.579]    [Pg.347]    [Pg.552]    [Pg.127]    [Pg.181]    [Pg.558]    [Pg.201]    [Pg.757]    [Pg.1023]    [Pg.395]    [Pg.438]    [Pg.133]    [Pg.145]    [Pg.150]    [Pg.226]   
See also in sourсe #XX -- [ Pg.193 , Pg.430 ]



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