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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992808Generated: October 26, 2026

1-(3-Methoxyphenyl)acetone → 1-(3-Methoxyphenyl)propan-2-ol

https://huagongshe.com/reaction/1992808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Methoxyphenyl)acetoneHCID 76410—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-(3-Methoxyphenyl)propan-2-olHCID 1249985299%

Reaction Steps

To a cold solution (5° C.) of 1-[3-(methyloxy)phenyl]-2-propanone (75 g, 0.457 mol) in MeOH (500 mL) was added NaBH4 (19 g, 0.502 mol) portion-wise over a period of 0.5 h. The resultant mixture was stirred at that temperature for 1 h. Reaction mixture was quenched with 1 N aqueous HCl (250 mL) and concentrated under reduced pressure to remove most of the methanol. The reaction mixture was extracted with EtOAc (3×150 mL). The combined organic layer was washed with water (1×100 mL), brine (1×100 mL), dried (Na2SO4) and concentrated under reduced pressure to afford the crude product. The reaction mixture was just passed through a pad of silica gel and washed with 1:1 hexanes:EtOAc to afford 75 g (99%) of the title compound. 1H NMR (400 MHz, CDCl3): δ 7.24-7.20 (m, 1H), 6.80-6.75 (m, 3H), 4.02-3.97 (m, 1H), 3.79 (s, 3H), 2.78-2.63 (m, 2H), 1.25-1.19 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649093B2
Source datasetuspto-grants-2010_01
ORD IDord-de7ef9ac13094006b14c9f4d7f2fafaf
Source noteuspto-grants-2010_01