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HRID 2260955作成日:2026年10月26日

Pentaerythritol → Mono-o-(phytanyl)pentaerythritol

https://huagongshe.com/reaction/2260955

反応式

関与物質

役割名称HCID仕込み量
反応物PentaerythritolHCID 8285—
反応物Sodium hydrideHCID 24758—
反応物3,7,11,15-Tetramethyl-1-hexadecanol 4-MethylbenzenesulfonateHCID 20186185—
溶媒DimethylformamideHCID 6228—
生成物Mono-o-(phytanyl)pentaerythritolHCID 1169736422.8%

反応手順

Under a nitrogen gas stream, 36.09 g (265.1 mmol) of pentaerythritol was dissolved in 210 ml of dry DMF, and 5.3 g (132.5 mmol) of 60% NaH was added little by little under ice cooling. The resultant was heated to room temperature and agitated for 1 hour, and 30.0 g (66.26 mmol) of phytanyl tosylate was added dropwise thereto, followed by washing with 55 ml of DMF. The resultant was heated to 80° C. and agitated for 4 hours, the resulting reaction solution was concentrated under reduced pressure, 500 ml of ether was added to the residual solution to perform extractive dissolution twice, the product was washed twice with saturated saline, and then it was dried over anhydrous magnesium sulfate. After the filtration, the resultant was concentrated, purified by silica gel column chromatography to obtain 6.3 g of mono-O-(3,7,11,15-tetramethylhexadecyl)pentaerythritol, which was in colorless, transparent, and somewhat viscous liquid form. The purity of the product determined by HPLC analysis was not lower than 99.5%. The results of NMR analysis are as shown below.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07846903B2
出典データセットuspto-grants-2010_12
ORD IDord-49d880234d514920815a94701b30ce55
出典メモuspto-grants-2010_12