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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409364Generated: October 30, 2026

Beta-Alanine → HCID 86636691, compound

https://huagongshe.com/reaction/409364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-AlanineHCID 239—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 24730218HCID 24730218—
ReactantHCID 57994057HCID 57994057—
SolventAcetic AcidHCID 176—
ProductHCID 86636691HCID 86636691—

Reaction Conditions

Temperature170 °C

Reaction Steps

To a mixture of 2-(5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid (0.031 g, 0.117 mmol) and 5-(4-trifluoromethoxy-phenyl)thiophene-2-carbaldehyde (0.030 g, 0.117 mmol) in acetic acid 5 mL is added β-alanine (1.042 mg, 0.012 mmol) and heat to 170° C. for 30 min under microwave irradiation. The resulting reaction mixture is cooled down and the solvent is removed. The pure product (0.035 g, 0.069 mmol, red solid) is obtained by column chromatography using MeOH/DCM, 2-7% ration solvent system. 1H-NMR (CD3OD/300 MHz): 7.91 (m, 2H), 7.32 (d, J=9.0 Hz, 2H), 7.14 (m, 5H), 7.02 (m, 2H), 6.47 (s, 1H), 5.64 (dd, J=11.1, 5.4 Hz, 11H), 3.70 (dd, J=14.1, 12.6 Hz, 1H), 3.53 (dd, J=14.1, 5.1 Hz, 1H). MS (ES−, m/z): 501.4 (M−, 100.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759384B2
Source datasetuspto-grants-2014_06
ORD IDord-ee85277a7edd4c5a99322da8e9697d0c
Source noteuspto-grants-2014_06