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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989813Generated: October 29, 2026

Hydrochloric Acid → 5-Dibutylamino-2-methoxy-benzaldehyde

https://huagongshe.com/reaction/1989813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDibutylamineHCID 8148—
ReactantSodium HydroxideHCID 14798—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-(5-Bromo-2-methoxyphenyl)-1,3-dioxaneHCID 14378759—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product5-Dibutylamino-2-methoxy-benzaldehydeHCID 8588890646%

Reaction Conditions

Temperature25 °C

Reaction Steps

2-(5-Bromo-2-methoxy-phenyl)-[1,3]dioxane (40 mmol), di-n-butylamine (48 mmol), Pd2(dba)3 (0.2 mmol, 1 mol % Pd), P(o-tol)3 (0.6 mmol) and Na-t-OBu (68 mmol) was stirred in degassed toluene (60 mL) at 80° C. for 18 h. The darkbrown mixture was poured into icecold hydrochloric acid (1 M, 200 mL) and stirred vigorously for 2 hours at 25° C. The solution was cooled to 0° C. and pH was adjusted to 9 using 6M NaOH(aq) and extracted with Et2O (4×100 mL). The organic phase was dried (Na2SO4) and the solvent was removed under reduced pressure. The resulting crude oil purified by flash chromatography using EtOAc/n-heptane (1:4, v/v) as eluent. The product was isolated as yellow oil in 46% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642367B2
Source datasetuspto-grants-2010_01
ORD IDord-8261bab93a224a1980c3988478e40b97
Source noteuspto-grants-2010_01