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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066443Generated: November 1, 2026

Hydrochloric Acid → HCID 178516421, compound

https://huagongshe.com/reaction/2066443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(3,4-Dichlorophenyl)hydrazineHCID 83161—
ReactantPropionate ionHCID 104745—
ReactantPotassium tert-butoxideHCID 23665647—
ProductHCID 178516421HCID 17851642137%

Reaction Steps

N′-(3,4-Dichlorophenyl)hydrazine was liberated from its hydrochloride (8.7 g, 40.6 mmol) by partitioning the solid between dilutes Na2CO3 solution and ethyl acetate. The aqueous layer was extracted 2 more times with AcOEt, dried over Na2SO4 and the solvent removed in vacuo. The residue is taken up in t-butyl alcohol (60 ml) and, in a dry nitrogen atmosphere, the ethyle propionate (4.6 ml, 44.66 mmol) was dropwise added. The mixture was ice-cooled and potassium t-butoxide (10.5 g, 81.2 mmol) was slowly added over the time of 1 hr. The resulting mixture was stirred overnight at room temperature. The solvent was evaporated in vacuo and ice-water was added. The resulting aqueous solution is extracted with dichloromethane and acidified to pH 6 with acetic acid. The solid precipitated was filtered off, dried and crystallized from ethyl acetate yielding 2.4 g of brown solid. The mother liquors were evaporated to dryness and the crude residue was column chromatographied on silica gel (petroleum ether/AcOEt 9:1) another fraction of 1 g was obtained (total yield 37%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293740B2
Source datasetuspto-grants-2012_10
ORD IDord-c07e6761176046059bcea2626abe8929
Source noteuspto-grants-2012_10