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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626957Generated: November 2, 2026

Acetic Acid → HCID 61166465, compound

https://huagongshe.com/reaction/1626957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPivalaldehydeHCID 12417—
Reactant4-Methoxy-2-nitroanilineHCID 66793—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
ProductHCID 61166465HCID 61166465—

Reaction Steps

4-Methoxy-2-nitroaniline (10 g, 59.5 mmol, 1.0 equiv.) and trimethyl-acetaldehyde (9.73 g, 113 mmol, 1.9 equiv.) were dissolved in anhydrous DCM (100 ml). The resulting solution was treated with acetic acid (18.72 ml, 327 mmol, 5.5 equiv.), followed by sodium triacetoxyborohydride (30.3 g, 143 mmol, 2.4 equiv.). The reaction mixture was stirred at room temperature. When LCMS showed completion of the reaction, the reaction was quenched with saturated aqueous NaHCO3, then extracted with EtOAc. The combined organic layers were dried over Na2SO4 and concentrated to give N-(2,2-dimethylpropyl)-4-methoxy-2-nitroaniline (3), which was used without purification. LRMS m/z (M+H) 239.0 found, 238.1 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785481B2
Source datasetuspto-grants-2014_07
ORD IDord-89b14dd377e54c09b91470660f68fd0d
Source noteuspto-grants-2014_07