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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307909Generated: October 30, 2026

Ethyl Acetate → Ethyl 4-(m-methoxyphenyl)-3-phenyl-3-hydroxybutyrate

https://huagongshe.com/reaction/2307909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-(3-Methoxyphenyl)-1-phenylethan-1-oneHCID 2759614—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(m-methoxyphenyl)-3-phenyl-3-hydroxybutyrateHCID 2260268586%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Lithium hexamethyldisilazane (88.5 mL, 88.5 mmol) was added to THF (150 mL) at −78° C. After 15 min, ethyl acetate (7.79 g, 88.5 mmol) was added over 10 min and stirred at −78° C. for 30 min. The m-methoxybenzyl phenyl ketone in (10.0 g, 44.25 mmol) THF (100 mL) was added over 15 min and kept at that temperature for 3 h. The reaction mixture was quenched at that temperature with saturated ammonium chloride (15 mL). The reaction mixture was diluted with ether (200 mL) and the organic layer was washed with brine, (100 mL), dried and was concentrated to afford 12 g (86%) of the desired product. 1H NMR (CDCl3) δ 7.10-7.37 (m, 6H), 6.71-6.74 (m, 1 H), 6.60-6.62 (m, 1 H), 6.48 (s, 1 H), 3.95-4.00 (m, 2H), 3.67 (s, 3H), 2.72-3.07 (m, 4H), 1.06 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833366B1
Source datasetuspto-grants-2004_12
ORD IDord-c89c9eece0954ccb90a04a581a9fe930
Source noteuspto-grants-2004_12