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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133110Generated: November 1, 2026

4-Tert-Butylaniline → 2-[2-(4-Tert-butyl-phenylamino)-ethyl]-6-nitro-benzoic acid methyl ester

https://huagongshe.com/reaction/133110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Tert-ButylanilineHCID 69861—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Nitro-6-(2-oxoethyl)benzoic Acid Methyl EsterHCID 86690692—
SolventDichloromethaneHCID 6344—
Product2-[2-(4-Tert-butyl-phenylamino)-ethyl]-6-nitro-benzoic acid methyl esterHCID 69159152—

Reaction Steps

To a solution of the aldehyde (Step B, 0.51 g, 2.3 mmol, 1 eq) and CH2Cl2 (30 mL) was added 4-t-butyl-aniline (0.36 mL, 2.3 mmol, 1 eq) and NaBH(OAc)3 (1.5 g, 6.8 mmol, 3.0 eq). The mixture was stirred at RT for 18 h then quenched with H2O. The mixture was extracted with EtOAc, the organic layer was washed with brine, dried (MgSO4) and concentrated in vacuo to give an orange oil. Purification by silica flash chromatography gave the desired compound as a yellow-orange foam. MS m/e 357 (M+H)+. Calc'd for C20H24N2O4-356.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390820B2
Source datasetuspto-grants-2008_06
ORD IDord-19c51f58e8fc491a97da71dd17bc8f8c
Source noteuspto-grants-2008_06