HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660843Generated: October 25, 2026
Diethyl Ether → 2-(3-bromobenzoyl)-N-isobutylhydrazinecarboxamide
https://huagongshe.com/reaction/660843
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Methylpropyl isocyanate | HCID 61281 | — |
| Reactant | m-Bromobenzohydrazide | HCID 520941 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-bromobenzoyl)-N-isobutylhydrazinecarboxamide | HCID 47428167 | — |
Reaction Steps
5.00 g (23.3 mmol) of 3-bromobenzoic acid hydrazide are placed in 50 ml tetrahydrofuran at room temperature. 2.70 g (27.2 mmol) of isobutyl isocyanate, dissolved in 10 ml tetrahydrofuran, are rapidly added dropwise with stirring to this suspension. The mixture is firstly further stirred at room temperature and then allowed to stand overnight. The precipitate formed after addition of 100 ml diethyl ether is filtered off and then washed with diethyl ether. An initial quantity of 1.42 g (19% of theory) of the target compound is thus obtained. The mother liquor is concentrated, and the residue again slurried in diethyl ether and filtered. After washing with diethyl ether and drying in vacuo, a further 5.62 g (77% of theory) of the target compound remain.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084481B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-3f37f4fe9ad4464197e67393f814bb5e |
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| Source note | uspto-grants-2011_12 |
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