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HRID 602232作成日:2026年10月25日

Tetraethoxysilane → Tetraethoxysilane

https://huagongshe.com/reaction/602232

反応式

関与物質

役割名称HCID仕込み量
反応物TetraethoxysilaneHCID 6517—
反応物1,4,8,11-Tetraazacyclotetradecane, 1,4,8,11-tetramethyl-HCID 123502—
反応物HCID 178468048HCID 178468048—
溶媒WaterHCID 962—
生成物TetraethoxysilaneHCID 6517—
生成物Germanium monoxideHCID 6327639—

反応手順

1.01 g tetraethylorthosilicate, 2.0 g deionized water, and 0.41 g germanium ethoxide were mixed together in a tared 23 mL Teflon liner. Then 0.42 g of 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane (Strem Chemicals) was dissolved in the mixture. The Teflon container was then capped, sealed, and placed within an 23-mL steel Parr autoclave. The autoclave was allowed to remain at room temperature for 2 days during which time the TEOS and germanium ethoxide were allowed to hydrolyze. The Teflon cup was then removed from the autoclave and 0.13 g 50% HF was added and mixed to create a white viscous gel. The ethanol (formed from the hydrolysis of the TEOS and germanium oxide) and water were allowed to evaporate within a vented hood with flowing air over the course of 3-4 days. Sufficient water was added and mixed into the gel to bring the molar ratio H2O/(Si+Ge) to 7. The liner was then capped and placed within a Parr Steel autoclave reactor. The autoclave was then fixed in a rotating spit within an oven heated at 160° C. for 10 days. The solid products were recovered from the cooled reactor by vacuum filtration and washed with copious quantities of water.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906101B2
出典データセットuspto-grants-2011_03
ORD IDord-8d44390428f44ba6a6ed232acbbc61e3
出典メモuspto-grants-2011_03