HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293063Generated: October 25, 2026
Octadecyldimethylchlorosilane → Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanine
https://huagongshe.com/reaction/2293063
Participants
| Role | Name | HCID | Charge |
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| Reactant | Octadecyldimethylchlorosilane | HCID 87738 | — |
| Reactant | HCID 178526211 | HCID 178526211 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanine | HCID 137226509 | — |
Reaction Steps
[In analogy to a procedure by Wheeler et. al., J. Am. Chem. Soc. 106, 7404 (1984)] 3.3 g (9.5 mmol) of dimethyl-octadecyl-chlorosilane and 0.5 g (0.8 mmol) of dihydroxygermanium-phthalocyanine in 50 ml of pyridine are stirred for 2 hours at 50°. The solution is cooled and filtered using a suction filter. The solvent is removed in vacuo, and 250 ml of hexane are added to the residue. The resulting precipitate is filtered off with suction and washed first with hexane, then in portions with 200 ml of acetone/water (1:1). The residue is dried overnight under a high vacuum, then extracted with toluene in a Soxhlet, freed of solvent and dried, yielding bis(dimethyl-octadecyl-siloxy)germanium-phthalocyanine; NMR (pyridine-d5): δ=9.8-9.9 (m, 8H); 8.3-8.5 (m,8H): aromatic H's; 0.75-1.46 (various m's); 0.45(m); -0.03 (m); -0.88 (m); -1.91 (m); -2.48 (m, 4×CH3 : silyl side chains) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686439 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-3fa59259dee8400f8fe09fa55377eceb |
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| Source note | uspto-grants-1997_11 |
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