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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046898Generated: November 1, 2026

Dimethylformamide → 6-Methoxy-1-methyl-3,4-dihydro-2-naphthaldehyde

https://huagongshe.com/reaction/2046898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium AcetateHCID 517045—
Reactant7-methoxy-4-methyl-1,2-dihydronaphthaleneHCID 11829938—
Product6-Methoxy-1-methyl-3,4-dihydro-2-naphthaldehydeHCID 1369444244%

Reaction Conditions

Temperature72.5 °C

Reaction Steps

To a solution of Compound B (0.44 g, 2.5 mmole) in dry dimethylformamide (1.3 ml, 16.8 mmole) at ice cooling and stirring under argon atmosphere, phosphorus oxychloride (0.62 ml, 6.65 mmole) was added drop-by-drop in 2 minutes. The reaction mixture was stirred in an oil bath of 70-75° C. for 3 hours. After cooling in an ice bath, ice (6 g) was added, then sodium acetate (anhydrous, 3.7 g) was added, and the mixture (pH ˜6) was warmed in an oil bath at 70-75° C. for 15 minutes. After cooling, it was extracted with ether (1×10 ml and 3×5 ml), the combined organic solutions were washed with water (3×3 ml), dried (magnesium sulfate), decolorized (with activated carbon), and evaporated. The residue (0.33 g) was recrystallized from cyclohexane (2 ml) and dried over potassium hydroxide in a vacuum giving the pure product 6-Methoxy-1-methyl-3,4-dihydro-2-naphthaldehyde (Compound C, 0.22 g, 44%) as light brown crystals, mp. 70-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592458B2
Source datasetuspto-grants-2013_11
ORD IDord-961b812cbe8f4a7b8416553ffa44e2d0
Source noteuspto-grants-2013_11