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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343170Generated: October 30, 2026

Acetone → HCID 54250348, compound

https://huagongshe.com/reaction/343170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant2-MethoxyanilineHCID 7000—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54250348HCID 54250348119.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium triacetoxyborohydride (27.9 g, 134 mmol) is added portionwise over 45 minutes to a 0° C. solution of 2-methoxyaniline (12.5 g, 101 mmol) in THF (100 mL), acetone (7.82 mL, 106 mmol) and acetic acid (5.9 mL) and the resultant mixture is allowed to attain RT overnight. The reaction mixture is cooled to 0° C. and then water (50 mL) is added slowly followed by 50% aqueous sodium hydroxide solution (20 mL) and the resultant mixture stirred for 1.5 h. The organics were removed and the residual aqueous phase diluted with water (30 mL) and extracted into ethyl acetate (3×50 mL). The combined organics were washed with water (2×100 mL), brine (50 mL), dried (MgSO4) and concentrated in vacuo to afford N-Isopropyl-N-(2-methoxy-phenyl) aniline (14.51 g) as an amber oil which is used without further purification: 1H NMR (300 MHz, CDCl3) δ6.91 (t, 1H, J=7.6), 7.01 (d, 1H, J=7.6), 6.68 (t, 2H, J=7.9), 3.88 (s, 3H), 3.66 (m, 1H, J=6.8), 1.28 (d, 6H, J=6.8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859007
Source datasetuspto-grants-1999_01
ORD IDord-6eb44edc23d84c5aaf47dee198ca67b2
Source noteuspto-grants-1999_01