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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968121Generated: October 29, 2026

Dimethylformamide → HCID 22291738, compound

https://huagongshe.com/reaction/968121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantClopyralidHCID 15553—
ReactantHCID 19374211HCID 19374211—
SolventWaterHCID 962—
ProductHCID 22291738HCID 2229173851%

Reaction Steps

3,6-Dichloropyridine-2-carboxylic acid (1.0 g, 5.23 mmol.), sodium hydroxide (1.64 g, 15.7 mmol.), and anhydrous THF (10 mL) were combined before slowly adding the N,N-dimethylaminoethanethiol (1.9 g, 18.3 mmol). After stirring for several hours under nitrogen, two aliquots of DMF (10 mL each) were added. Several hours later, additional DMF (10 mL) and dimethylaminoethanethiol (1.9 g, 18.3 mmol) were added. The reaction was stirred overnight at room temperature. The solution was diluted with water and extracted three times with methylene chloride. The aqueous was acidified to pH 5 and extracted four times with methylene chloride. The aqueous was acidified to pH 1, the solvent was removed, and the residue was recrystallized from hot water. Yellow solid, 0.786 g (51% yield). 1H NMR (300 MHz, CD3OD): δ 2.98 (s, 6H), 3.53 (m, 4H), 7.50 (d, 1H), 7.85 (d, 1H). 13C NMR (75 MHz, CD3OD): δ 24.4, 42.8, 58.2, 125.7, 128.1, 140.0, 147.3, 158.2, 166.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956052B2
Source datasetuspto-grants-2005_10
ORD IDord-56fb97eeb60c4f0481474c2410485563
Source noteuspto-grants-2005_10