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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614315Generated: November 3, 2026

Triethylamine → HCID 54534971, compound

https://huagongshe.com/reaction/1614315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-BromobenzaldehydeHCID 70741—
Reactant2-(5-Methyl-2-nitrophenyl)acetic acidHCID 14740976—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 54534971HCID 5453497199%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a mixture of 4-bromobenzaldehyde (19.5 g, 106 mmol) and 2-nitro-5-methyl-phenylacetic acid (20.6 g, 106 mmol; J. G. Atkinson et. al., Tetrahedron Lett., 2857, 1979) in 100 ml of acetic anhydride was added triethylamine (14.7 ml, 106 mmol) and the resulting reddish solution was heated at 40° C. for 70 hours. Most of the acetic anhydride was evaporated under vacuum and the residue was diluted with ethyl acetate and washed with sat. NH4Cl, H2O, and brine. Drying (MgSO4) and evaporation yielded 37.87 g (99%) of product as a yellow solid which was used in the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196529
Source datasetuspto-grants-1993_03
ORD IDord-b334f0dbdeef4abca7cbd5089e6c23f2
Source noteuspto-grants-1993_03