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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340845Generated: October 30, 2026

Triethylamine → HCID 14084268, compound

https://huagongshe.com/reaction/340845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
SolventTolueneHCID 1140—
ProductHCID 14084268HCID 14084268—

Reaction Steps

About 6.02 g of ethyl glycinate hydrochloride, 14.39 g of triethylamine, and 10 ml of toluene were mixed in a round-bottom reaction flask cooled with an ice bath. To this mixture was added, in a dropwise fashion, a solution of 21.1 g of trimethylsilyl trifluoromethanesulfonate in 50 ml of toluene. The resulting mixture was stirred at room temperature for 19 hours to give a biphasic mixture. The top layer was transferred to another flask, and the bottom layer was extracted with 40 ml of toluene. The combined toluene solution was evaporated under vacuum. The residue was extracted with 100 ml of hexane, and the hexane layer was evaporated under vacuum, yielding ethyl [bis(trimethylsilyl)amino]acetate, also known as ethyl N,N-bis(trimethylsilyl)glycinate (BTMSEG), as a colorless liquid (9.23 g, 87% yield). The 1H NMR data (C6D6, 25° C., referenced to tetramethylsilane) of the product are listed as follows: δ 3.89 (quartet, 2 H, OCH2 protons), 3.51 (singlet, 2 H, NCH2 protons), 0.90 (triplet, 3 H, CH3 protons), 0.14 (singlet, 18H, Si—CH3 protons). From the 1H NMR data, the structure of the product was determined to be as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895670B2
Source datasetuspto-grants-2014_11
ORD IDord-fb8369684f324f03a2fa47997f895da9
Source noteuspto-grants-2014_11