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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367004Generated: October 30, 2026

Dimethylformamide → 2-Benzyloxy-3-(dimethylamino)acrolein

https://huagongshe.com/reaction/367004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantBenzyloxyacetaldehyde diethyl acetalHCID 4321487—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
Product2-Benzyloxy-3-(dimethylamino)acroleinHCID 5452100246.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Prepared by a modification of the literature procedure reported in Croat. Chim. Acta, 1966, 235. Phosphorus pentachloride (0.13 mol) was added to benzyloxyacetaldehyde diethyl acetal (0.13 mol) at 20-30° C. The reaction mixture was heated at 60° C. for 75 min and then cooled to 0° C. The reaction mixture was treated with DMF (0.39 mol) and stirred at room temperature for four days. The reaction mixture was diluted with 1.0N HCl(aq) (200 ml) and ether (200 ml). The ether layer was discarded and the aqueous layer was basified with 8N NaOH(aq). The aqueous layer was extracted with ethyl acetate and ether and the combined organic extracts were dried (MgSO4), filtered and evaporated in vacuo. The resulting black oil was purified by column chromatography to give the product as a brown solid (0.06 mol, 43%). δH (250 MHz; CDCl3) 8.62 (1H, s), 7.44-7.26 (5H, m), 6.18 (1H, s), 4.96 (2H, s), 3.04 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133255
Source datasetuspto-grants-2000_10
ORD IDord-ed877cb23e834ebe854cfc56067d845a
Source noteuspto-grants-2000_10