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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393877Generated: October 29, 2026

Dimethylformamide → 3,4-Dimethoxynaphthalene-1-carbaldehyde

https://huagongshe.com/reaction/393877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1,2-dimethoxynaphthaleneHCID 299257—
Solvent1,4-DichlorobenzeneHCID 4685—
Product3,4-Dimethoxynaphthalene-1-carbaldehydeHCID 1349555468.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1,2-dimethoxynaphthalene (0.74 g, 4 mmol) and DMF (0.8 mL, 10 mmol) in dichlorobenzene (0.8 mL) was stirred with POCl3 at 100° C. for 2 h. The reaction mixture was cooled to 0° C., quenched with a cold aqueous solution of NaOAc, diluted with H2O and extracted with benzene. The extracts were dried (MgSO4), concentrated and in vacuo and dichlorobenzene was removed by kugelrohr distillation at 110° C./0.5 mm Hg. Column chromatography (20%EtOAc in hexane) gave the product 18 (596 mg, 68%), which was used in the following step without further purification. 1H NMR (CDCl3) 10.42 (s, 1H), 9.00-9.15 (m, 1H), 8.15-8.30 (m, 1H), 7.61 (s, 1H), 7.50-7.65 (m, 2H), 4.12 (s, 3H), 4.07 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809176B2
Source datasetuspto-grants-2004_10
ORD IDord-ca5e6166279145b6b6043871e22970f8
Source noteuspto-grants-2004_10