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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382546Generated: October 30, 2026

Thionyl Chloride → HCID 22736697, compound

https://huagongshe.com/reaction/382546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-(2,5-dimethylthiophen-3-yl)prop-2-enoic AcidHCID 5712502—
SolventBenzeneHCID 241—
ProductHCID 22736697HCID 22736697—

Reaction Steps

To a solution of (E)-3-(2,5-dimethylthiophene-3-yl)acrylic acid (328 mg, 1.8 mmol) in benzene (10 ml) was added thionyl chloride (0.5 ml) and the mixture was heated to reflux for 60 min. Volatiles were removed by evaporation to give crude (E)-3-(2,5-dimethylthiophene-3-yl)acryloyl chloride. Free base of the titled compound was prepared from N-(2-pyridyl)-o-phenylenediamine (250 mg, 1.4 mmol) and (E)-3-(2,5-dimethylthiophene-3-yl)acryloyl chloride obtained as above according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). The free base was dissolved with a 10% methanol solution of hydrogen chloride (5 ml). Concentration and recrystallization from ethyl acetate/ethanol yielded the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310079B1
Source datasetuspto-grants-2001_10
ORD IDord-cbb76a7495614e03a0a5e4790b762903
Source noteuspto-grants-2001_10