Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359811Generated: October 27, 2026

Diisopropylamine → 5-(7-Bromoheptyl)-3-methylisoxazole

https://huagongshe.com/reaction/359811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant3,5-DimethylisoxazoleHCID 9312—
Reactant1,6-DibromohexaneHCID 12368—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-(7-Bromoheptyl)-3-methylisoxazoleHCID 13316967—

Reaction Conditions

Temperature-50 °C

Reaction Steps

To a stirred solution of 46.1 ml of diisopropylamine in 100 ml of tetrahydrofuran at 0°-5° C. was added 126 ml of 2.6M n-butyllithium in hexane over a period of about 20 minutes. The mixture was cooled to -50° C., 31.95 g of 3,5-dimethylisoxazole was added and the mixture stirred for 30 minutes. The latter mixture was cooled to -78° C. and 101.6 ml of 1,6-dibromohexane was added dropwise. After the addition was complete, the temperature of the reaction mixture was allowed to rise to room temperature and kept there for about 40 hours. Saturated aqueous ammonium chloride solution was then added and the mixture extracted with ethyl acetate. The ethyl acetate extracts were dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was distilled to remove excess dibromide (b.p. 50° C., 0.5 mm) and suspended in hexane. The suspension was decolorized with charcoal, filtered and cooled in a refrigerator overnight. The mixture was filtered and the filtrate concentrated in vacuo to give 57 g of 5-(7-bromoheptyl)-3-methylisoxazole as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002960
Source datasetuspto-grants-1991_03
ORD IDord-2a9a86bb33564c68bf432259c5c74bd3
Source noteuspto-grants-1991_03