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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12906Generated: October 25, 2026

Toluene → N'-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester

https://huagongshe.com/reaction/12906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium HydroxideHCID 14797—
Reactanttert-Butyl carbazateHCID 70091—
Reactant1-Bromo-3-methoxypropaneHCID 524551—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
ProductN'-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl esterHCID 8661530298%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of hydrazinecarboxylic acid tert-butyl ester (4.67 g, 27.16 mmol) in toluene (90 mL) was added pulverized potassium hydroxide (1.98 g, 35.3 mmol) and tetrabutylammonium hydrogensulfate (904 mg, 2.72 mmol). The solution was heated to 50° C. in a preheated oil bath and 1-bromo-3-methoxypropane (3.67 mL, 32.6 mmol) was added drop-wise over 45 minutes. The solution was then heated to 80° C. for 3 h. The solution was cooled to room temperature and washed with water (3×150 mL) until the water layer was neutral. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to provide N′-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester as a viscous oil (6.49 g, 98%), which was used without further purification. Mass spectrum: m/z: 245.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-25c3b70965af461399f9fca20de6164c
Source noteuspto-grants-2010_06