Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 136473082 | HCID 136473082 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 136365464 | HCID 136365464 | 83.9% |
Reaction Steps
10 g of dimethoxysilicon phthalocyanine synthesized in Synthesis Example 2 was added to 5 g of water and 95 g of N-methylpyrrolidone (95% NMP aqueous solution) and reacted at 120° C. for 3 hours. The reaction product was thermally filtrated and washed with NMP and acetone in the order named. After the product was stirred in 100 ml of acetone at room temperature, crystals were separated by filtration and dried to obtain 8.0 g of dihydroxysilicon phthalocyanine. When structural analysis was carried out by mass spectral (negative measurement) and IR (KBr method) methods, the same spectrum as that of Example 1 was obtained. Therefore, it was confirmed that the product was dihydroxysilicon phthalocyanine. The results of elemental analysis are shown below and almost agree with calculation values.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057071 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-aea1a9cc7e1e465e8d8cbd2e22fd1ce8 |
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| Source note | uspto-grants-2000_05 |
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