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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | tert-Butyl carbazate | HCID 70091 | — |
| Reactant | 1-Bromo-3-methoxypropane | HCID 524551 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Product | N'-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester | HCID 86615302 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728029B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-25c3b70965af461399f9fca20de6164c |
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| Source note | uspto-grants-2010_06 |
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