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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948731Generated: October 31, 2026

Acetic Acid → HCID 67199091, compound

https://huagongshe.com/reaction/1948731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl malonateHCID 7943—
ReactantPiperidineHCID 8082—
Reactant2-Amino-3-methoxybenzaldehydeHCID 13970121—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 67199091HCID 6719909161.3%

Reaction Steps

To a solution/suspension of 2-amino-3-methoxybenzaldehyde (1.8 g, 11.9 mmol) in dry toluene (30 mL) under nitrogen was added acetic acid (0.1 mL) followed by dimethyl malonate (3.4 mL, 29.8 mmol) and piperidine (2.9 mL, 29.8 mmol). The reaction mixture was heated at reflux for 2 h. After cooling to r.t., the mixture was diluted with water (30 mL) and extracted with EtOAc (2×150 mL). The organic layer was separated, dried (Na2SO4), filtered and concentrated in vacuo. The residue was triturated in EtOAc/Et2O and the resulting solid was filtered off and dried in vacuo to give the title compound (1.7 g, 61%) as a pale yellow solid. δH (DMSO-d6) 10.65 (br s, 1H), 8.52 (s, 1H), 7.42 (d, J 8.0 Hz, 1H), 7.27 (d, J 8.0 Hz, 1H), 7.21 (t, J 6.0 Hz, 1H), 3.94 (s, 3H), 3.84 (s, 3H). LCMS (ES+) 234 (M+H)+, RT 2.13 minutes (Method 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399483B2
Source datasetuspto-grants-2013_03
ORD IDord-bf60c2d96d68471588977af39a5a5371
Source noteuspto-grants-2013_03