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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516175Generated: November 4, 2026

Hydrazine hydrate (1:1) → HCID 178514444, compound

https://huagongshe.com/reaction/1516175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178501283HCID 178501283—
Solvent1-ButanolHCID 263—
ProductHCID 178514444HCID 17851444483%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of trans-4-(3-fluoro-pyridin-2-yloxy)-cyclohexanecarboxylic acid methyl ester (0.60 g, 2.4 mmol) and hydrazine hydrate (0.53 ml, 11 mmol) in n-butanol (1 ml) was heated at 125° C. for 4 h. After cooling to room temperature the reaction mixture was partitioned between dichloromethane (75 ml) and water (75 ml). The aqueous layer was washed with dichloromethane/75 ml). The combined organic layers were washed with water (75 ml) and brine (75 ml), dried over anhydrous sodium sulfate and concentrated in vacuo to give the crude title compound (0.45 g, 83%) as white solid, which was used in the next step without further purification. MS m/e: 254 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227458B2
Source datasetuspto-grants-2012_07
ORD IDord-c31a9e66035b4a76aac4ca767314a105
Source noteuspto-grants-2012_07