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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118211Generated: October 26, 2026

Water → 1-[4-(Methoxymethoxy)phenyl]-2-phenylbutan-1-one

https://huagongshe.com/reaction/2118211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-4-(methoxymethoxy)benzeneHCID 10465919—
ReactantN-methoxy-N-methyl-2-phenylbutanamideHCID 11229537—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-[4-(Methoxymethoxy)phenyl]-2-phenylbutan-1-oneHCID 5887766180%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 13 (99.0 g, 0.46 mol) in anhydrous THF (750 mL) was added n-BuLi (1.6 M in hexanes, 310 mL, 0.50 mol) dropwise at −78° C. The reaction mixture was stirred for 30 min and 14 (90.1 g, 0.43 mol) dissolved in THF (500 mL) was added dropwise. The reaction mixture was stirred at −78° C. for 1 h and then slowly warmed to 0° C. H2O (500 mL) was added and the volatiles were removed under reduced pressure. The residue was extracted with Et2O (3×500 mL) and the combined extracts were washed with water (500 mL) and brine (500 mL). The mixture was dried over MgSO4 and concentrated. The residue was recrystallized from hexanes to afford 97.6 g (80%) of 15 as white needles. 1HNMR (400 MHz, DMSO-d6): δ 0.79 (t, J=7.3 Hz, 3H), 1.68 (h, J=7.0 Hz, 1H), 2.03 (h, J=7.0 Hz, 1H), 3.32 (s, 3H), 4.65 (t, J=7.3 Hz, 1H), 5.21 (s, 2H), 7.03 (d, J=8.8 Hz, 2H), 7.15 (t, J=7.1 Hz, 1H), 7.23-7.30 (m, 4H), 7.98 (d, J=8.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442833B2
Source datasetuspto-grants-2008_10
ORD IDord-ca876288d4d643b6b27e67bd9dea86a2
Source noteuspto-grants-2008_10