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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323310Generated: October 30, 2026

Water → HCID 22009080, compound

https://huagongshe.com/reaction/323310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantHCID 18464680HCID 18464680—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 22009080HCID 22009080—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Combine 1-(3,4,5-trimethoxybenzyl)-3-(2-(t-butyldimethylsilyloxy)ethyl)-2-oxopyrrolidine (0.31 g, 0.74 mmol) and tetrahydrofuran (2 mL). Cool to −78° C. using a dry-ice/acetone bath. Add a solution of sec-butyllithium (0.63 mL, 1.3 M in hexane, 0.81 mmol). After 30 minutes, add a solution of 3,5-di(trifluoromethyl)benzyl bromide (0.25 g, 0.81 mmol) in tetrahydrofuran (1 mL). After 2 hours, warm to ambient temperature. After 12 hours, add water (10 mL). Separate the layers and extract the aqueous layer three times with ethyl acetate. Dry the combined organic layers over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 1/4 ethyl acetate/hexane to give the title compound: Rf=0.44 (silica gel, 1/4 ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-9dc6ef72b0684b4e9371b02f4097a1fe
Source noteuspto-grants-2001_04