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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990834Generated: October 30, 2026

Dimethylformamide → 3-Acetimido-5-ethoxy-4-iodo-benzaldehyde

https://huagongshe.com/reaction/1990834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Amino-5-ethoxy-4-iodo-benzaldehydeHCID 58706353—
Product3-Acetimido-5-ethoxy-4-iodo-benzaldehydeHCID 8660763135%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 3-amino-5-ethoxy-4-iodo-benzaldehyde (0.27 g, 0.93 mmol, 1.0 equiv; intermediate 25) and acetyl chloride (0.138 mL, 0.153 g, 1.95 mmol, 2.1 equiv) in anhydrous DMF (5 mL) was added diisopropylethylamine (0.48 mL, 0.36 g, 2.78 mmol, 3.0 equiv) and the mixture stirred at 50° C. for 48 h. Removal of the solvent under reduced pressure and purification of the crude reaction mixture with column chromatography on silica eluting with a gradient of heptane/ethyl acetate (4:1→1:1) yielded 0.11 g (35%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 1.51 (t, J=7.0 Hz, 3H), 2.29 (s, 3H), 4.19 (q, J=7.0 Hz, 2H), 7.06 (s, 1H), 7.76 (br s, 1H), 8.42 (s, 1H), 9.96 (s, 1H). MS (ISP): 334.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645753B2
Source datasetuspto-grants-2010_01
ORD IDord-71931424d0eb4a34b0e442b6632551d7
Source noteuspto-grants-2010_01