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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859979Generated: October 30, 2026

Diisopropylamine → HCID 18625922, compound

https://huagongshe.com/reaction/1859979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant4-Benzyloxybenzyl chlorideHCID 70042—
ReactantHCID 18625754HCID 18625754—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 18625922HCID 18625922—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of n-butyllithium in hexane (1.65M, 19.4 ml) was added dropwise over a period of 20 minutes at −60° C. to a solution of diisopropylamine (3.23 g) in anhydrous tetrahydrofuran (60 ml). The mixture was stirred at 0° C. for 30 minutes. To this mixture a solution of 2-methyl-5-phenylvalerate (7.05 g) in anhydrous tetrahydrofuran (30 ml) was added dropwise over a period of 20 minutes at −70° C. and the mixture was stirred at −70° C. for 40 minutes. To this reaction mixture a solution of 4-benzyloxybenzyl chloride (9.68 g) in anhydrous tetrahydrofuran (80 ml) was added dropwise at −70° C. The mixture was stirred at −70° C. for 3 hours. At the end of this time the reaction mixture was partitioned between ethyl acetate and water. The ethyl acetate layer was separated and washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified via chromatography on a silica gel column using hexane/ethyl acetate=15/1 as the eluant to afford the desired compound (1.88 g) as a syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528525B1
Source datasetuspto-grants-2003_03
ORD IDord-b4a8723293da4306a82f90472d25258b
Source noteuspto-grants-2003_03