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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514589Generated: October 27, 2026

Methylhydrazine → 2,5-dimethoxythiobenzoic acid N-methylhydrazide

https://huagongshe.com/reaction/514589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2,5-Dimethoxybenzoic acidHCID 76027—
ReactantLawesson's reagentHCID 87949—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2,5-dimethoxythiobenzoic acid N-methylhydrazideHCID 11333617116.8%

Reaction Steps

DCC (4.5 g, 21.8 mmol) was added in one portion to a solution of 2,5-dimethoxybenzoic acid (3.6 g, 20 mol), methylhydrazine (1.2 ml, 23 mmol) and DMAP (30 mg, cat.) in CH2Cl2 (60 ml) cooled in an ice bath. The reaction mixture was stirred overnight at room temperature. The slurry was cooled at −20° C. for 1 h and filtered. The CH2Cl2 solution was evaporated and the residue was dried in vacuum. The resulting crude product was dissolved in toluene (50 ml). To this solution was added Lawesson's reagent (5.8 g, 14 mmol). The mixture was refluxed for 40 min, cooled to room temperature, and directly subjected to silica gel column chromatography (eluent: 25% to 35% ethyl acetate in hexanes) to give the 2,5-dimethoxythiobenzoic acid N-methylhydrazide (3.7 g, yield: 82%) as off-white solid. 1H NMR (300 MHz, CDCl3): δ 6.88-6.80 (m, 3H), 5.46 (s, 2H), 3.84 (s, 3H), 3.82 (s, 3H), 3.28 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107955B2
Source datasetuspto-grants-2015_08
ORD IDord-7966abd067854db4a6f96b9cbe43e2d9
Source noteuspto-grants-2015_08