Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656808Generated: October 29, 2026

Diisopropylamine → 2-Fluoro-2-methyl-1-tetralone

https://huagongshe.com/reaction/1656808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant2-Methyl-1-tetraloneHCID 102650—
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantLithium diisopropylamineHCID 45051747—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-2-methyl-1-tetraloneHCID 1501445650%

Reaction Steps

0.16 milliliter diisopropylamine in 10 milliliters tetrahydrofuran were allowed to stand with 1.15 equivalents butyllithium at -25° C. The resulting solution of lithium diisopropylamine was cooled to -78° C. and 1 equivalent 2-methyl-1-tetralone in 5 milliliters tetrahydrofuran solution was dropped in. The mixture was allowed to stand at -70° C. for 100 minutes. 1.5 equivalents N-fluorobenzenesulfonimide prepared according to Example 1 above in 11 milliliters tetrahydrofuran were mixed rapidly with the mixture at -95° C. The mixture was quenched with 30 milliliters ammonium chloride solution and extracted with dichloromethane. The organic phase was dried with magnesium sulfate, filtered, and evaporated. 2-methyl-2-fluoro-tetralone was obtained in 50% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254732
Source datasetuspto-grants-1993_10
ORD IDord-225051308dab4752838f27b03d9e6062
Source noteuspto-grants-1993_10