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HRID 521302作成日:2026年10月27日

2,2,7,7-Tetramethyl-3,6-dioxa-2,7-disilaoctane → 2-(2,2-Dimethyl-3-nitropropyl)-2-methyl-[1,3]dioxolane

https://huagongshe.com/reaction/521302

反応式

関与物質

役割名称HCID仕込み量
反応物2,2,7,7-Tetramethyl-3,6-dioxa-2,7-disilaoctaneHCID 81858—
反応物4,4-Dimethyl-5-nitropentan-2-oneHCID 4156383—
触媒Trimethylsilyl triflateHCID 65367—
溶媒DichloromethaneHCID 6344—
生成物2-(2,2-Dimethyl-3-nitropropyl)-2-methyl-[1,3]dioxolaneHCID 1463805197.2%

反応手順

A stirred solution of 1,2-bis(trimethylsilyloxy)ethane (26.5 g, 128 mmol) in dichloromethane (50 mL) was cooled in a dry ice/isopropanol bath, and trimethylsilyl trifluoromethanesulfonate (2.2 g, 1.0 mmol) was added, followed by the dichloromethane solution of 4,4-dimethyl-5-nitropentan-2-one (50 mL, 19.0 g, 119 mmol) from the previous step. After 30 minutes, the cooling bath was removed and the solution was allowed to warm to room temperature. The solution was filtered through a plug of potassium carbonate and concentrated under reduced pressure to provide 2-(2,2-dimethyl-3-nitropropyl)-2-methyl-[1,3]dioxolane (23.5 g) as a dark oil that was used directly in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328110B2
出典データセットuspto-grants-2016_05
ORD IDord-cc8b8aaf51d44583aafc7dd54d21a15e
出典メモuspto-grants-2016_05