Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220462Generated: October 30, 2026

Methylhydrazine → ethyl 3-(1,3,5-trimethyl-1H-pyrazol-4-yl)propanoate

https://huagongshe.com/reaction/220462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantHexanoic acid, 4-acetyl-5-oxo-, ethyl esterHCID 2733934—
SolventAcetic AcidHCID 176—
Productethyl 3-(1,3,5-trimethyl-1H-pyrazol-4-yl)propanoateHCID 1639480993%

Reaction Steps

Dissolve ethyl 4-acetyl-5-oxohexanoate (2.00 g, 9.99 mmol) in acetic acid (21 mL). Add methyl hydrazine (589 μL, 10.99 mmol) and stir at room temperature for 18 hr. Concentrate and dissolve residue in ethyl acetate. Wash ethyl acetate layer with saturated aqueous sodium bicarbonate solution. Extract aqueous layer twice with ethyl acetate, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 0:100 to 100% ethyl acetate:hexanes) to give 3-(1,3,5-trimethyl-1H-pyrazol-4-yl)-propionic acid ethyl ester (1.95 g, 93%). MS (ES): m/z=211 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-000c6f90b8f246098496a859eabe70f4
Source noteuspto-grants-2012_06