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HRID 257104생성일: 2026년 10월 26일

Triethylamine → (R)-3-[(1,1-dimethylethyl)dimethylsilyloxy]tetradecanoic acid

https://huagongshe.com/reaction/257104

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Triethylamine hydrochlorideHCID 11130—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물3R-hydroxymyristic acid methyl esterHCID 9834945—
촉매4-(Dimethylamino)pyridineHCID 14284—
촉매tert-Butyldimethylsilyl chlorideHCID 28928—
용매DichloromethaneHCID 6344—
생성물(R)-3-[(1,1-dimethylethyl)dimethylsilyloxy]tetradecanoic acidHCID 54310188103.5%

반응 단계

50 g of methyl (R)-3-hydroxytetradecanoate, 35 g of t-butyldimethylchlorosilane, 6.1 g of 4-dimethylaminopyridine and 29.4 g of triethylamine were dissolved in 200 ml of methylene chloride and stirred at room temperature for 30 hours as well as under reflux for 16 hours. Thereupon, a further 2 g of t-butyldimethylchlorosilane were added. After a further 24 hours under reflux the precipitated triethylamine hydrochloride salt was filtered off, washed with ether and the filtrate was concentrated. The residue was dissolved in ether and washed in sequence with water, 0.5M citric acid, again with water and saturated sodium chloride solution, dried, concentrated and subsequently freed from volatile material at 5° C. in a high vacuum for 5 hours. There were obtained 71.8 g of (R)-3-[(1,1-dimethylethyl)dimethylsilyloxy]tetradecanoic acid, IR (cm-1): 1745, 1254, 895, 776.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05260310
출처 데이터셋uspto-grants-1993_11
ORD IDord-7f6241b608384da19a8444e2067669df
출처 메모uspto-grants-1993_11