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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493075Generated: October 30, 2026

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

https://huagongshe.com/reaction/1493075

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 numberUS05376674
Source datasetuspto-grants-1994_12
ORD IDord-cf10120928e947759c2f577533e52e00
Source noteuspto-grants-1994_12