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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579218Generated: November 4, 2026

Thionyl Chloride → HCID 21568139, compound

https://huagongshe.com/reaction/1579218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-PyridinemethanamineHCID 31018—
ReactantHCID 21568136HCID 21568136—
SolventBenzeneHCID 241—
ProductHCID 21568139HCID 21568139—

Reaction Steps

To 15 g of 2,10-dichloro-12H-dibenzo[d,g][1,3]dioxocin-6-carboxylic acid was added 75 ml of thionyl chloride, and the heterogenous mixture was refluxed with occasional stirring until it became homogenous. The mixture was refluxed for an additional 2 hours after which the thionyl chloride was distilled off under reduced pressure affording a solid residue which was dissolved in 300 ml of dry benzene by warming on a steam bath. The benzene was distilled off under reduced pressure affording a white crystalline residue to which was added 500 ml of dry benzene. The mixture was stirred at room temperature until homogenous then 35 g of 3-aminomethylpyridine was added. After standing at room temperature for 2 hours the mixture was heated to reflux for an additional 3 hours, cooled to room temperature, poured into ice water and separated. Methanol was added to aid the solubility of the product in the organic layer. The organic layer was washed with water and distilled under reduced pressure resulting in a residue which was dried and recrystallized twice from methanol-acetone (1:1) to give the desired product, M.P. 225°-226°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931173
Source datasetuspto-grants-1976_01
ORD IDord-663c4236920d4229b376220658b75e77
Source noteuspto-grants-1976_01