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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732029Generated: October 26, 2026

Methoxyacetic Acid → N-ethyl-2-(methoxyacetyl)hydrazinecarbothioamide

https://huagongshe.com/reaction/732029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetic AcidHCID 12251—
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Ethyl-3-thiosemicarbazideHCID 1551780—
ReactantThiosemicarbazideHCID 2723789—
ReactantHCID 178418300HCID 178418300—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-ethyl-2-(methoxyacetyl)hydrazinecarbothioamideHCID 327417647%

Reaction Steps

Methoxyacetic acid 360 mg, 3.99 mmol), 4-ethyl-3-thiosemicarbazide (581 mg, 4.87 mmol), diisopropylcarbodiimide (615 mg, 4.87 mmol) and hydroxybenzotriazole (69.6 mg, 0.51 mmol) were mixed in dimethylformamide (10 ml) and stirred under argon at ambient temperatures for 19 h. After evaporation to dryness the crude was used directly in the next step. MS (ESI) m/z 192 (M+1). Step 2: 4-Ethyl-5-methoxymethyl-2,4-dihydro-[1,2,4]triazole-3-thione: N-Ethyl-2-(methoxyacetyl(hydrazinecarbothioamide (760 mg crude, 4 mmol) and sodium bicarbonate (560 mg, 6.6 mmol) were suspended in water (15 ml) and refluxed for 5 h. After cooling and filtration the filtrate was acidified with concentrated hydrochloric acid, followed by extraction with ethyl acetate. After evaporation to dryness the crude was recrystallized in ethyl acetate/heptane. Filtration and recrystallization of the mother liquor gave a combined yield of 325 mg (47%) of the title compound. 1H NMR (CDCl3), δ (ppm): 4.47 (s, 2H), 4.13 (q, 2H), 3.37 (s, 3H), 1.38 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585881B2
Source datasetuspto-grants-2009_09
ORD IDord-b7a079693fad4ce4b900f5573574d456
Source noteuspto-grants-2009_09