HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546694Generated: November 1, 2026
Trifluoroacetic acid → 5-Chloro-2-cyclopropyl-valeric acid hydrazide
https://huagongshe.com/reaction/546694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-butyl N'-(5-chloro-2-cyclopropyl-pentanoyl)-hydrazinecarboxylate | HCID 66839486 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Chloro-2-cyclopropyl-valeric acid hydrazide | HCID 66839471 | 93.1% |
Reaction Steps
Trifluoroacetic acid (0.5 ml) was added to a solution of tert-butyl N′-(5-chloro-2-cyclopropyl-pentanoyl)-hydrazinecarboxylate (208 mg) in methylene chloride (1 ml) under ice-cooling, and then the reaction solution was stirred at room temperature for two hours. A saturated sodium bicarbonate solution and ethyl acetate were added to the reaction solution, and the organic layer was separated. The organic layer was sequentially washed with a saturated sodium bicarbonate solution and brine. The combined aqueous layers were reextracted with ethyl acetate (twice). The combined organic layers were dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain 127 mg of the title compound. The property values of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935815B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-9546f6b11fa249eca34854bf8d1c10ef |
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| Source note | uspto-grants-2011_05 |
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