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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847086Generated: October 30, 2026

Triethylamine → HCID 19815326, compound

https://huagongshe.com/reaction/847086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Benzyloxybenzyl chlorideHCID 70042—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 19815326HCID 1981532650.5%

Reaction Steps

To a suspension of 11.0 g of glycine ethyl ester hydrochloride in 100 mL of dimethylformamide at 25° was added 22.0 mL of triethylamine. To the resulting milky suspension was added 9.08 g of 4-benzyloxybenzyl chloride in 50 mL of DMF dropwise over 0.5 hour. The mixture was stirred for 16 hours at 25°. The reaction mixture was diluted with diethyl ether and then filtered to remove the precipitated triethylamine hydrochloride. The resultion solution was concentrated in vacuo, and the residue was dissolved in ethyl acetate. The solution was washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated. Kugelrohr distillation provided 5.90 g of N-(4-benzyloxybenzyl)glycine ethyl ester [bp 160°-180° (0.015 torr.)]; NMR (200 MHz, CDCl3): δ7.43-7.27 (m, 5H); 7.06 (A2B2, 4H); 5.01 (s, 2H); 4.14 (quart., 2H); 3.71 (s, 2H); 3.36 (s, 3H); 2.01 (bs, 1h); 1.24 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05138069
Source datasetuspto-grants-1992_08
ORD IDord-4df5a90c097c4f2fac634f628df1854d
Source noteuspto-grants-1992_08