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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348737Generated: October 26, 2026

Dipropylamine → [3-(6-t-Butyldimethylsilyloxymethylnaphthalen-2-yl)propyl]dipropylamine

https://huagongshe.com/reaction/348737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDipropylamineHCID 8902—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(6-t-Butyldimethylsilyloxymethylnaphthalen-2-yl)propionaldehydeHCID 23079194—
SolventMethanolHCID 887—
Product[3-(6-t-Butyldimethylsilyloxymethylnaphthalen-2-yl)propyl]dipropylamineHCID 23079316103.6%

Reaction Steps

Dipropylamine (363 mg) was dissolved in anhydrous methanol (20 ml) and then added with sodium cyanoborohydride (281 mg), trimethyl orthoformate (0.490 ml), and the compound (981 mg) obtained in Example 121-7, followed by stirring overnight at room temperature under a nitrogen atmosphere. After completion of the reaction, the solvent was distilled off. Then, the residue was dissolved in chloroform and added with a saturated aqueous sodium bicarbonate solution, followed by stirring. The solution was extracted with chloroform and the extract was then washed with a saturated aqueous sodium bicarbonate solution and saturated saline solution. After that, the organic layer was dried with anhydrous sodium sulfate. Subsequently, the solvent was distilled off and the residue was then purified through silica gel column chromatography (chloroform/ethyl acetate), thereby obtaining the subject compound (1.28 g) as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176227B2
Source datasetuspto-grants-2007_02
ORD IDord-0718d365aefe4eb38e5d790838d53d10
Source noteuspto-grants-2007_02