HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198659Generated: November 1, 2026
Methanol → Ethyl valerate carbethoxyhydrazone
https://huagongshe.com/reaction/1198659
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Hydrazinecarboxylic acid, ethyl ester | HCID 20064 | — |
| Reactant | Ethyl pentanimidate hydrochloride | HCID 12283341 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl valerate carbethoxyhydrazone | HCID 53752329 | — |
Reaction Steps
To a solution of 7.0 g (25.3 mmole) of ethyl valerimidate hydrochloride [prepared by method of A. J. Hill and I. Rabinowitz, J. Am. Chem. Soc., 48, 734 (1926)] in 35 ml of dry ethanol stirred under N2 at -78° C. was added dropwise a solution of 24 g (23 mmole) of ethyl carbazate in 35 ml of dry ethanol. Precipitation occurred during the addition, which took 20 minutes and was accompanied by a rise in the internal temperature to -50° C. The mixture was allowed to stand at 5° C. for 60 hours and then filtered. The filtrate was concentrated, and the residue was flash chromatographed on a silica gel column (elution with 98.5:1.5 CH2Cl2 --MeOH), yielding a clear oil, homogeneous by TLC in 97:3 CH2Cl2 --MeOH; mass spectrum (FAB) m/e 217 (M+1)+. NMR suggested a mixture of syn and anti isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05281614 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-0c1ea9c7c1e84f4c96efbe7770fbcc91 |
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| Source note | uspto-grants-1994_01 |
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