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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257104Generated: October 26, 2026

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

https://huagongshe.com/reaction/257104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriethylamine hydrochlorideHCID 11130—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3R-hydroxymyristic acid methyl esterHCID 9834945—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Catalysttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDichloromethaneHCID 6344—
Product(R)-3-[(1,1-dimethylethyl)dimethylsilyloxy]tetradecanoic acidHCID 54310188103.5%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260310
Source datasetuspto-grants-1993_11
ORD IDord-7f6241b608384da19a8444e2067669df
Source noteuspto-grants-1993_11