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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218351Generated: October 25, 2026

Methanol → Methyl 5-[(2E)-3-(dimethylamino)prop-2-enoyl]-2-methoxybenzoate

https://huagongshe.com/reaction/218351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantMethyl 5-acetyl-2-methoxybenzoateHCID 606426—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-[(2E)-3-(dimethylamino)prop-2-enoyl]-2-methoxybenzoateHCID 5801547790.1%

Reaction Conditions

Temperature95 °C

Reaction Steps

Methyl 5-acetyl-2-methoxybenzoate (11.98 g, 48.0 mmol) was added to N,N-dimethylformamide dimethyl acetal (44.6 g, 374.5 mmol) held under a nitrogen atmosphere. The resulting solution was heated at 95° C. for 60 minutes. Methanol (10 ml) was then removed by atmospheric distillation and further N,N-dimethylformamide dimethyl acetal (8.90 g, 74.9 mmol) added. The resulting solution was heated at 95° C. for a further 270 minutes. The reaction was then cooled to 50° C. and ethyl acetate (35 mL) added. Solvent (35 mL) is removed from the reaction by atmospheric distillation and fresh ethyl acetate (35 mL) added. Further solvent (35 mL) is removed from the reaction by atmospheric distillation and fresh ethyl acetate (50 mL) added. The reaction mixture is cooled to RT whereby the desired product crystallises out as a granular, free flowing solid. The solid was isolated by filtration, washed twice with fresh ethyl acetate (2×30 mL) and dried to constant weight to afford 11.39 g of the desired methyl 5-[(2E)-3-(dimethylamino)prop-2-enoyl]-2-methoxybenzoate (8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198441B2
Source datasetuspto-grants-2012_06
ORD IDord-8e86a24c94064261b40e8b03092a0b64
Source noteuspto-grants-2012_06