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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822380Generated: November 1, 2026

Hydrochloric Acid → HCID 57893430, compound

https://huagongshe.com/reaction/1822380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68812564HCID 68812564—
ReactantHCID 68813589HCID 68813589—
ProductHCID 57893430HCID 5789343044%

Reaction Steps

Ethyl 5-hydroxy-3-oxo-2-(phenylmethyl)-6-(trifluoromethyl)-2,3-dihydro-4-pyridazinecarboxylate. Sodium hydride (0.040 g of a 60% oil suspension, 1.00 mmol) was added to a stirred solution of ethyl 5-hydroxy-3-oxo-6-(trifluoromethyl)-2,3-dihydro-4-pyridazinecarboxylate (0.083 g, 0.329 mmol) in dimethylformamide (1.5 mL) under nitrogen. After 10 min stirring at room temperature, the mixture was cooled in an ice bath and benzyl bromide (0.043 mL, 0.362 mmol) injected. The mixture was stirred for 3 h at 0° C. 0.1M aqueous hydrochloric acid (50 mL) was added and the mixture extracted with ethyl acetate. The extracts were washed with water and brine, then dried (MgSO4), evaporated under reduced pressure and the residue chromatographed (silica gel, 5-10% methanol dichloromethane) to give the title compound (0.050 g, 44%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.23 (t, J=6.95 Hz, 3H) 4.17 (q, J=7.07 Hz, 2H) 5.14 (s, 2H) 7.12-7.44 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608621B2
Source datasetuspto-grants-2009_10
ORD IDord-23cf325e47c749e293250bc6ea9b2a8d
Source noteuspto-grants-2009_10