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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2260955생성일: 2026년 10월 26일

Pentaerythritol → Mono-o-(phytanyl)pentaerythritol

https://huagongshe.com/reaction/2260955

반응식

참여 물질

역할이름HCID투입량
반응물PentaerythritolHCID 8285—
반응물Sodium hydrideHCID 24758—
반응물3,7,11,15-Tetramethyl-1-hexadecanol 4-MethylbenzenesulfonateHCID 20186185—
용매DimethylformamideHCID 6228—
생성물Mono-o-(phytanyl)pentaerythritolHCID 1169736422.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07846903B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-49d880234d514920815a94701b30ce55
출처 메모uspto-grants-2010_12