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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610371Generated: October 31, 2026

Sodium Chloride → HCID 10923477, compound

https://huagongshe.com/reaction/610371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantBenzyl BromideHCID 7498—
ReactantDiisopropylamineHCID 7912—
ReactantHexamethylphosphoramideHCID 12679—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Methoxy-1,2,3,4-tetrahydronaphthalen-1-oneHCID 81276—
ReactantLithium diisopropylamideHCID 2724682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10923477HCID 1092347726.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a -78° C. solution of lithium diisopropyl amide (from 43.8 ml (0.312 mol) of diisopropyl amine in 280 ml tetrahydrofuran and 119 ml (0.298 mol) of 2.5 M n-butyllithium) was slowly added a solution of 50 g (0.285 mol) of 7-methoxy-3,4-dihydro-1(2H)-naphthalenone in 100 ml tetrahydrofuran. The resultant reaction mixture was stirred 10 minutes at -78° C. The cooling bath was charged to a 0° C. ice bath, followed immediately by the rapid addition of 38 ml (0.32 mol) of benzyl bromide. Hexamethylphosphoramide (106 ml, 0.60 mol) was then added and the resultant solution stirred at 25° C. for 2 hours. The reaction was added to saturated NH4Cl and saturated NaCl, dried over MgSO4, and evaporated to an oil, which was purified via column chromatography on 1 Kg of silica gel eluted with 10% ether-hexane to give 20 g (26%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998451
Source datasetuspto-grants-1999_12
ORD IDord-5c228a974e82420eb504e4c9dc36f3a5
Source noteuspto-grants-1999_12