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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115580Generated: October 31, 2026

Methylhydrazine → 2,5-dimethoxythiobenzoic acid N-methylhydrazide

https://huagongshe.com/reaction/2115580

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 (300MHz, 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 numberUS07435843B2
Source datasetuspto-grants-2008_10
ORD IDord-490cf6b717ff469fadd66309ffe56ec1
Source noteuspto-grants-2008_10