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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607029Generated: October 31, 2026

Triethylamine → HCID 53872938, compound

https://huagongshe.com/reaction/1607029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantp-Toluenesulfonyl azideHCID 13661—
Reactant(4-nitrophenyl)methyl 3-oxobutanoateHCID 2760918—
SolventAcetonitrileHCID 6342—
ProductHCID 53872938HCID 53872938—

Reaction Conditions

Temperature0 °C

Reaction Steps

35.0 ml (0.25 mol-1.8 equiv.) of triethylamine were added dropwise to a solution, cooled to 0° C., of 33.18 g (0.14 mol) of 4-nitrobenzyl acetoacetate and 30.40 g (0.15 mol) of p-toluenesulphonyl azide in 280 ml of anhydrous acetonitrile. The mixture was stirred at 0° C. for 2 hours, and the resultant precipitate was then filtered off under suction, washed with ether and dried in a high vacuum over P4O10. 20.3 g (55% of theory) of the title compound were obtained as colorless crystals, melting point: 132° C. A further 6.3 g (17% of theory) of the title compound were obtained by chromatography of the filtrate solution on 400 g of silica gel (toluene:ethyl acetate=9:1), Rf =0.35 (toluene:ethyl acetate=9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863916
Source datasetuspto-grants-1989_09
ORD IDord-6cdd6c9cc45c42ec9bc1c2d5c74a8cb6
Source noteuspto-grants-1989_09