反応式
[CH:1]([OH:5])([CH2:3][CH3:4])[CH3:2].[CH2:6]([C:10]([CH3:12])=[O:11])[CH:7](C)C.[CH3:13][C:14]([O:16][CH2:17][CH2:18]OC)=[O:15]>>[C:14]([O:16][CH2:17][CH3:18])(=[O:15])[CH2:13][CH3:1].[C:14]([O:16][CH2:17][CH2:18][O:11][CH2:10][CH3:12])(=[O:15])[CH3:13].[C:1]1(=[O:5])[CH2:2][CH2:7][CH2:6][CH2:4][CH2:3]1参加物
実験手順
Examples of the high boiling organic solvents are phthalic acid alkyl esters (e.g., dibutyl phthalate, dioctyl phthalate, etc.), phosphoric acid esters (e.g., diphenyl phosphate, triphenyl phosphate, tricresyl phosphate, dioctylbutyl phosphate, etc.), citric acid esters (e.g., tributyl acetylcitrate, etc.), benzoic acid esters (e.g., octyl benzoate, etc.), alkylamides (e.g., diethyllaurylamide, etc.), fatty acid esters (e.g., dibutoxyethyl succinate, dioctyl azelate, etc.), trimesic acid esters (e.g., tributyl trimesate, etc.), etc. Also, examples of the low boiling organic solvents are organic solvents having a boiling point of about 30° C. to 160° C., such as lower alkyl acetates (e.g., ethyl acetate, butyl acetate, etc.), ethyl propionate, secondary butyl alcohol, methyl isobutyl ketone, β-ethoxyethyl acetate, methyl cellosolve acetate, cyclohexanone, etc. The dye providing substance is dissolved in the aforesaid high boiling organic solvent or the low boiling organic solvent and then dispersed in a hydrophilic colloid. In this case, a mixture of the high boiling organic solvent and the low boiling organic solvent may be used.
出典と根拠
- ORDレコード
- ord-9cf019d2c22e49c3994fa0334fd2d176
- 出典データセット
- uspto-grants-1987_09
- 特許番号
- US04695525
関連ノート
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