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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839366Generated: October 29, 2026

Hydrochloric Acid → HCID 21948210, compound

https://huagongshe.com/reaction/1839366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantVinylidene chlorideHCID 6366—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2,6-Dichlorpyridine-3-carbonyl chlorideHCID 12263984—
SolventDichloromethaneHCID 6344—
ProductHCID 21948210HCID 2194821068.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of the 2,6-dichloro-nicotinoyl chloride (1.0 g, 4.76 mmol) from the previous reaction in CH2Cl2 (5 mL) was added slowly to a cooled (0° C.) and stirred slurry solution of AlCl3 (0.64 g, 4.76 mmol) in CH2Cl2 (20 mL). After 15 min, vinylidene chloride (0.38 mL, 0.46 g, 4.76 mmol) was added to the mixture dropwise. The reaction was allowed to warm to room temperature and was stirred overnight. The mixture was then poured over ice and was acidified using 1 N HCl (15 mL). Stirring was continued for 20 min and the product was extracted with CH2Cl2 (3×). The combined organic extracts were dried over Na2SO4 and concentrated in vacuo to give 3,3-dichloro-1-(2,6-dichloro-3-pyridinyl)-2-propen-1-one (0.88 g, 68% ) as a light yellow oil: 1H-NMR (CDCl3, 300 MHz) δ8.38, d, J=8.4, 1H). 7.40 (d, J=8.4, 1H), 7.10 (s, 1H); Rf=0.5 (4:1 Hex:EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677352B1
Source datasetuspto-grants-2004_01
ORD IDord-9c60e7ebf2454b88af79e4c0352dff94
Source noteuspto-grants-2004_01