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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754165Generated: November 4, 2026

Potassium Carbonate → N'-(2,3-dimethyl-benzoyl)-hydrazinecarboxylic acid, tert-butyl ester

https://huagongshe.com/reaction/1754165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl carbazateHCID 70091—
Reactant2,3-Dimethylbenzoyl chlorideHCID 2800899—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN'-(2,3-dimethyl-benzoyl)-hydrazinecarboxylic acid, tert-butyl esterHCID 59838585101.7%

Reaction Steps

T-butylcarbazate (35.15 g, 266 mmol) and 200 mL of CH2Cl2 were added to a round bottom flask. Potassium carbonate (55.2 g, 0.4 moles) dissolved in 350 mL of water was added to the flask, and the mixture was stirred for 15 minutes with ice chilling. 2,3 dimethylbenzoyl chloride (44.9 g, 266 mmol) in ca. 200 mL of CH2Cl2 was added drop-wise from a 500 mL separatory funnel over 30 minutes. The reaction was allowed to stir overnight and then the reaction mixture was poured into a 1 L separatory funnel and the CH2Cl2 phase was separated. Then ca. 150 mL of water was added, and the mixture was extracted twice with 150 mL of CHCl3. The combined organic phase was back-extracted with 100 mL of water, then with 1N HCl (250 mL), to remove the hydrazide. The organic phase was dried, stirred with charcoal, and the solvent removed in vacuo to yield a light tan solid (71.5 g) of N′-(2,3-dimethyl-benzoyl)-hydrazinecarboxylic acid, tert-butyl ester. 1H NMR (300 MHz, CHCl3) δ (ppm): 7.7 (br, 1H), 7.22 (m, 2H), 7.1 (t, 1H), 7.85 (br, 1H), 2.35 (s, 3H), 2.3 (s, 3H), 1.5 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169210B2
Source datasetuspto-grants-2015_10
ORD IDord-61dabfb7250e4bc690d10f53cd4b2404
Source noteuspto-grants-2015_10