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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365526Generated: October 31, 2026

Acetic Acid → N-Isopropyl-3-broMoaniline

https://huagongshe.com/reaction/365526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
Reactant3-BromoanilineHCID 11562—
ReactantSodium AcetateHCID 517045—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductN-Isopropyl-3-broMoanilineHCID 23291934—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (16.5 g, 435 mmol) was added slowly over 2 hours to a mixture of 3-bromoaniline (10 g, 58.13 mmol), ethanol (58 mL), acetic acid (50 mL, 866.1 mmol), water (140 mL), acetone (35 mL, 482.5 mmol), and sodium acetate (15.8 g, 116.2 mmol). The solution was stirred at 0° C. for 3 hours. The reaction mixture was poured into 1:1 mixture of ether and hexane containing 2N KOH. The layers were separated and the aqueous layer was extracted with ether/hexane (1:1). The combined organic layers were washed once with water and brine, dried with MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (10% ethyl acetate in hexane, Rf=0.31) to give the title compound (23.10 g, 93% as an oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127382
Source datasetuspto-grants-2000_10
ORD IDord-69262a77297e40e0ad93be9708005277
Source noteuspto-grants-2000_10