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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077265Generated: November 3, 2026

N-Pentylhydrazine → HCID 76629633, compound

https://huagongshe.com/reaction/2077265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-PentylhydrazineHCID 14247—
ReactantEthyl oxoacetateHCID 70211—
SolventEthanolHCID 702—
ProductHCID 76629633HCID 7662963397.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a magnetically stirred solution of oxo-acetic acid ethyl ester (35.08 ml, 177 mmol; 50% solution in toluene) in ethanol (450 ml) was added n-pentylhydrazine (21.7 g, 212 mmol) and the resulting solution was heated at 80° C. for 16 hours. The obtained mixture was allowed to attain room temperature and concentrated. The resulting residue was taken up in ethylacetate and water. The organic layer was separated and subsequently dried over MgSO4, filtered and concentrated to give (pentylhydrazono)acetic acid ethyl ester (Intermediate II-1) (32.2 gram, 93% yield) as a purple colored oil. 1H-NMR (400 MHz, CDCl3) δ 0.87-0.94 (m, 3H), 1.25-1.42 (m, 7H), 1.55-1.68 (m, 2H), 3.17-3.23 (m, 1H), 3.35-3.45 (m, 1H), 4.28 (q, J=7, 2H), 6.51 (br s, 1H), 6.72 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928134B2
Source datasetuspto-grants-2011_04
ORD IDord-3902c89133f54e07afd1a99e5611efde
Source noteuspto-grants-2011_04