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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604233Generated: October 25, 2026

Diethyl Ether → 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide

https://huagongshe.com/reaction/1604233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCyclohexaneHCID 8078—
ReactantMagnesium BromideHCID 82241—
ReactantN-ethyl-1-naphthalenecarboxamideHCID 4088726—
Reactantt-Butylperoxy benzoateHCID 21744378—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
Product2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamideHCID 1960231933%

Reaction Steps

A solution of 1.3M s-BuLi in cyclohexane (34 mL, 44 mmol) was added dropwise to a -78° C. cooled solution of N-ethyl-1-naphthalenecarboxamide (20 mmol) and TMEDA (6.0 mL, 40 mmol) in THF (100 mL). After 30 min, MgBr2.Et2O (15.5 g, 60 mmol) was added portion wise, and the reaction was briefly warmed to ambient temperature then was recooled to -78° C. After 1 h at -78° C., t-butylperoxy benzoate (4.3 g, 22 mmol) was added. The resulting reaction was warmed to -30° C. and worked up in the usual manner, then was purified by chromatography with 3:7 ethyl acetate/hexanes to afford 1.7 g of desired compound as a white solid, a 33% yield. m.p. 126-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994270
Source datasetuspto-grants-1999_11
ORD IDord-9c54fa92272446849c5eb0d3d0b99cd6
Source noteuspto-grants-1999_11