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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760828Generated: November 1, 2026

Sodium Chloride → Butyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-amine

https://huagongshe.com/reaction/1760828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantButyl iodideHCID 10962—
Reactant5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-amineHCID 11469760—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductButyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-amineHCID 2259684137%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-ylamine (1) (0.3 g, 1.5 mmole) in 30 mL tetrahydrofuran (THF) was cooled to −78° C. and 2.5 M n-butyllithium solution (0.6 mL) was added dropwise. The reaction mixture was allowed to warm to 0° C. over a one hour period. Iodobutane (0.171 mL) was added at 0° C. and the reaction mixture was stirred at room temperature for 15 hours. The reaction mixture was then poured into 50 mL of a saturated aqueous sodium chloride solution and extracted with three portions of 50 mL of ethyl acetate. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo to provide a brown oil. The product was purified by flash chromatography (SiO2, 5% ethyl acetate/hexanes) to provide 143 mg (37%) of butyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-amine (7) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06844466B2
Source datasetuspto-grants-2005_01
ORD IDord-a962307d7632400794896d4fea996b71
Source noteuspto-grants-2005_01