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HRID 1379003作成日:2026年10月25日

L-Selenocysteine → Bis(dimethyl-octadecyl-siloxy)germanium phthalocyanine

https://huagongshe.com/reaction/1379003

反応式

関与物質

役割名称HCID仕込み量
反応物L-SelenocysteineHCID 25076—
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. Sec. 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05670491
出典データセットuspto-grants-1997_09
ORD IDord-19f8da6eee6249d78df90e7691d9d5d2
出典メモuspto-grants-1997_09