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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409798Generated: October 30, 2026

Methyl 2-bromopropionate → HCID 140590449, compound

https://huagongshe.com/reaction/2409798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-bromopropionateHCID 95576—
ReactantSodium AcetateHCID 517045—
ReactantHCID 88851450HCID 88851450—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 140590449HCID 14059044930%

Reaction Conditions

Temperature60 °C

Reaction Steps

To (E)-N-(2-cyclopropylphenyl)-2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzylidene)hydrazinecarbothioamide (100 mg, 0.191 mmol) and sodium acetate (63.0 mg, 0.765 mmol) in EtOH (4 mL) was added methyl 2-bromopropanoate (0.026 mL, 0.230 mmol). The reaction was heated to 60° C. overnight. The reaction was then heated to 85° C. for 72 hours. The reaction mixture was diluted with DCM and washed with water. The aqueous layer was extracted with DCM. The organic layers were poured through a phase separator and concentrated. Purification by flash column chromatography provided the title compound as a white solid (32.5 mg, 0.056 mmol, 30%): mp 112-115° C.; 1H NMR (400 MHz, CDCl3) δ 8.58 (s, 1H), 8.32 (s, 1H), 8.22 (d, J=8.3 Hz, 2H), 7.87-7.75 (m, 4H), 7.43-7.32 (m, 4H), 7.26-7.24 (m, 2H), 4.23 (q, J=7.3 Hz, 1H), 1.85-1.78 (m, 4H), 0.90-0.78 (m, 2H), 0.78-0.69 (m, 1H), 0.65-0.55 (m, 1H); ESIMS m/z 578 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815922B2
Source datasetuspto-grants-2014_08
ORD IDord-47ebcf50775f4eb9862d545076472842
Source noteuspto-grants-2014_08