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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127573Generated: October 26, 2026

Triethylamine → HCID 53708924, compound

https://huagongshe.com/reaction/127573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(Bromomethyl)-1-chloro-3-nitrobenzeneHCID 91858—
Reactant(R)-Ethyl 2-amino-propionate hydrochlorideHCID 10236019—
SolventEthanolHCID 702—
ProductHCID 53708924HCID 5370892493.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 18.24 g of D-alanine ethyl ester hydrochloride in 60 ml of ethanol was added dropwise to a mixture of 25 ml of triethylamine in 60 ml of ethanol and the resulting mixture was heated to 80° C. The solution obtained was added dropwise at this temperature to a solution of 15 g of 2-chloro-6-nitrobenzyl bromide in 60 ml of ethanol. The mixture was stirred at 80° C. overnight and then evaporated to dryness. The residue was treated with 150 ml of deionised water and extracted twice with 100 ml of methylene chloride. The methylene chloride extracts were washed with water, dried over sodium sulphate and evaporated. The resulting product was purified by chromatography on silica gel with methylene chloride/5% methanol. There were obtained 16 g (93% of theory) of N-(2-chloro-6-nitrobenzyl)-D-alanine ethyl ester; nD25 =1.5247; [α]D =-6.9° (c=1% in ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256748
Source datasetuspto-grants-1981_03
ORD IDord-8f3631eba64e4d3b959b52004ebbed82
Source noteuspto-grants-1981_03