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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046252Generated: November 1, 2026

Hydrochloric Acid → HCID 57893424, compound

https://huagongshe.com/reaction/2046252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactantalpha-Bromo-o-chlorotolueneHCID 11905—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68812286HCID 68812286—
ReactantHCID 68812883HCID 68812883—
ProductHCID 57893424HCID 5789342466%

Reaction Steps

Ethyl 2-[(2-chlorophenyl)methyl]-5-hydroxy-3-oxo-6-phenyl-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-phenyl-2,3-dihydro-4-pyridazinecarboxylate (example 4(b), 0.100 g, 0.384 mmol) in dimethylformamide (1.5 mL) under nitrogen. After 15 min stirring at room temperature, the mixture was cooled in an ice bath and 2-chlorobenzyl bromide (0.051 mL, 0.384 mmol) injected. The mixture was stirred for 18 h while warming to room temperature, then poured into 0.1M aqueous hydrochloric acid (50 mL) and 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, 1-5% methanol/dichloromethane) to give the title compound (0.098 g, 66%) as a colourless gum. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.50 (t, J=7.20 Hz, 3H) 4.55 (q, J=7.07 Hz, 2H) 5.54 (s, 2 H) 7.20-7.28 (m, 3H) 7.35-7.52 (m, 4H) 7.75-7.84 (m, 2H) 13.83 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE044613E1
Source datasetuspto-grants-2013_11
ORD IDord-f99e8c9a733f4ea0810be5d93624cdd5
Source noteuspto-grants-2013_11