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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516159Generated: November 3, 2026

Hydrazine hydrate (1:1) → HCID 178514433, compound

https://huagongshe.com/reaction/1516159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178501260HCID 178501260—
ProductHCID 178514433HCID 17851443386%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of trans-4-(3-chloro-phenoxy)-cyclohexanecarboxylic acid methyl ester (0.25 g, 0.93 mmol) and hydrazine hydrate (0.044 ml, 0.91 mmol) was heated at 120° C. for 22 h. Addition of further hydrazine hydrate (0.020 ml, 0.42 mmol) was followed by stirring at 120° C. for 5 h. After cooling to room temperature the reaction mixture was partitioned between ethyl acetate (50 ml) and 1 M aqueous sodium hydroxide solution (50 ml). The layers were separated and the aqueous layer was extracted with a 50-ml portion of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give the crude title compound (0.21 g, 86%) as white solid, which was used in the next step without further purification. MS m/e: 269 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227458B2
Source datasetuspto-grants-2012_07
ORD IDord-9bcae4de9c4543ba981b731cc285a9d0
Source noteuspto-grants-2012_07