Complex compound and optical recording medium containing same
A technology of coordination compounds and protons, which is applied to optical record carriers, recording/reproducing by optical methods, data recording, etc., can solve the problems of insufficient moisture and heat resistance and other characteristics, and achieve the effect of excellent moisture and heat resistance.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0176] Hereinafter, the present invention will be described in more detail through synthesis examples, working examples, and test examples.
[0177] The description of the abbreviations is as follows.
[0178] TFP: 2,2,3,3-Tetrafluoropropanol
[0179] DMSO: dimethyl sulfoxide
[0180] [Manufacture of raw materials for compound (I)]
[0181] 1-Butyl- 3-cyano-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine. In the same manner as the production method of 1-butyl-3-cyano-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine, 3-cyano-1-iso Butyl-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine, 3-cyano-1-furfuryl-4-methyl-2,6-dioxo -1,2,5,6-tetrahydropyridine, 3-cyano-4-methyl-2,6-dioxo-1-(p-tolyl)-1,2,5,6-tetrahydropyridine , 1-butyl-3-cyano-2,6-dioxo-4-propyl-1,2,5,6-tetrahydropyridine, and 1-benzyl-3-cyano-4-methanol Base-2,6-dioxo-1,2,5,6-tetrahydropyridine. 3-cyano-1-ethyl-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine was obtained as a commercial item (manufactured by Sigma-Aldrich...
Synthetic example 1
[0191] Synthesis Example 1: Production of Compound (I-1)
[0192]1-Butyl-3-cyano-5-(N,N-dimethylaminomethylene)-4-methyl-2,6-dioxo-1,2,5,6-tetrahydro 1.50 g of pyridine, 1.05 g of acetic acid, 1.01 g of 5-hydrazino-1-phenyl-1H-tetrazole, and 15 ml of ethanol were mixed, and stirred at 70° C. for 1 hour. The reaction mixture was cooled to room temperature, 20 ml of water was added to the reaction mixture, the precipitated solid was collected by filtration, washed with a mixed solvent of water and ethanol (volume ratio 1:1), and dried to obtain compound (I-1) 1.47g (65% yield).
[0193] 1 H-NMR(400MHz)δ(DMSO-d 6 )ppm: 0.90(3H,t,J=7.3Hz), 1.25-1.30(2H,m), 1.46-1.51(2H,m), 2.35(3H,s), 3.83(2H,t,J=7.3Hz ), 7.56-7.67 (5H, m), 8.38 (1H, s).
Synthetic example 2
[0194] Synthesis Example 2: Production of Compound (I-2)
[0195] 3-cyano-5-(N,N-dimethylaminomethylene)-1-ethyl-4-methyl-2,6-dioxo-1,2,5,6-tetrahydro 0.50 g of pyridine, 1.05 g of acetic acid, 0.24 g of 2-hydrazinopyrimidine, and 5 ml of methanol were mixed and stirred at room temperature for 30 minutes. The precipitated solid was collected by filtration, washed with methanol, and then dried to obtain 0.61 g of compound (I-2) (95% yield).
[0196] 1 H-NMR(400MHz)δ(DMSO-d 6 )ppm: 1.10(3H,t,J=7.1Hz), 2.40(3H,s), 3.88-3.93(2H,m), 6.95(1H,bs), 8.36(1H,s), 8.54(2H,bs ), 11.13 (1H, bs).
PUM
| Property | Measurement | Unit |
|---|---|---|
| thickness | aaaaa | aaaaa |
| thickness | aaaaa | aaaaa |
| thickness | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 