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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323260Generated: October 30, 2026

Water → 1-(3,4,5-Trimethoxybenzyl)-3-(phenylmethyl)-2-oxopyrrolidine

https://huagongshe.com/reaction/323260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(3,4,5-Trimethoxybenzyl)-2-oxopyrrolidineHCID 18464662—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexaneHCID 21226206—
Product1-(3,4,5-Trimethoxybenzyl)-3-(phenylmethyl)-2-oxopyrrolidineHCID 18464420—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Combine 1-(3,4,5-trimethoxybenzyl)-2-oxopyrrolidine (1.0 g, 3.77 mmol) and tetrahydrofuran (5 mL). Cool to −78° C. using a dry-ice /acetone bath. Add a solution of lithium bis(trimethylsilyl)amide (4.25 mL, 1 M in THF, 4.52 mmol). After 30 minutes, add a solution of benzyl bromide (0.77 g, 4.52 mmol) in tetrahydrofuran (1 mL). After the addition of benzyl bromide is complete, warm slowly to ambient temperature. After 15 minutes, add water and extract three times with dichloromethane. Dry the combined organic layers over Na2SO4, filter, and concentrate in vacuo to obtain a residue. Chromatograph the residue on silica gel eluting with 1/1 ethyl acetate/hexane to give the title compound: Rf=0.69 (silica gel, 1/1 ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-dac7bf019398467abc12f501f05a4fd2
Source noteuspto-grants-2001_04