Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100650Generated: October 31, 2026

Acetic Acid → HCID 57799941, compound

https://huagongshe.com/reaction/2100650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl(methylene)ammounium iodideHCID 2724133—
ReactantHCID 57799935HCID 57799935—
ProductHCID 57799941HCID 57799941—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-(3-fluoro-2-methylphenyl)-1-(2-fluorophenyl)-5-(3-methoxyphenyl)pentane-1,5-dione (8.4 g, 20.6 mmol) and Eschenmoser's salt (17.6 g, 94.9 mmol) in acetic acid (86 mL) was stirred at 120° C. under nitrogen for 16 h. An additional 3.8 g (20 mmol) of Eschenmoser's salt was added and the mixture heated an additional 5 h. The solution was allowed to cool to room temperature and concentrated in vacuo. The residue was dissolved in EtOAc (30 mL) and 9:1 hexanes/EtOAc, and then treated with 10% NaOH until the pH reached 11 (150 mL). After 30 min, the resulting brown solid was collected by filtration, triturated with EtOAc (3×50 mL), and dried under vacuum at 40° C. to give 2-((dimethylamino)methyl)-3-(3-fluoro-2-methylphenyl)-1-(2-fluorophenyl)-5-(3-methoxyphenyl)-4-methylenepentane-1,5-dione product (7.5 g, 76% crude yield) as a yellow solid (characterized by LCMS and 1H NMR, LRMS (M+H+) m/z=478.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572814B2
Source datasetuspto-grants-2009_08
ORD IDord-542552d919cc42a5a934c73087c73d04
Source noteuspto-grants-2009_08