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HRID 1708359作成日:2026年10月25日

Octadecyldimethylchlorosilane → Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanine

https://huagongshe.com/reaction/1708359

反応式

関与物質

役割名称HCID仕込み量
反応物OctadecyldimethylchlorosilaneHCID 87738—
反応物HCID 178526211HCID 178526211—
溶媒PyridineHCID 1049—
生成物Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanineHCID 137226509—

反応手順

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 fast 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05358940
出典データセットuspto-grants-1994_10
ORD IDord-877c980e1c9d4a3bb90424c6a8b25e4d
出典メモuspto-grants-1994_10