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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563850Generated: October 31, 2026

Hydrazine → [1-(4-Trifluoromethoxyphenyl)-methylidene]-hydrazine

https://huagongshe.com/reaction/563850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactantp-(Trifluoromethoxy)benzaldehydeHCID 69573—
SolventEthanolHCID 702—
Product[1-(4-Trifluoromethoxyphenyl)-methylidene]-hydrazineHCID 6667978891%

Reaction Steps

Hydrazine (3.3 mL, 105 mmol) was dissolved in ethanol (10 mL) at room temperature. To this solution was added 4-trifluoromethoxybenzaldehyde (5.0 mL, 35 mmol) dropwise over 25 min. The reaction mixture was stirred an additional 45 min and concentrated under vacuum. The residue was dissolved in ethyl ether (20 mL) and washed with water (10 mL). The water layers were extracted with ethyl ether (3×15 mL), and the combined organic layer was dried over magnesium sulfate, filtered and concentrated to give [4-(trifluoromethoxy)benzylidene]hydrazine (XX) as a yellow oil (6.5 g, 91% yield). 1H NMR (DMSO-d6): δ 7.69 (s, 1H); δ 7.56 (d, J=8.7 Hz, 2H) δ 7.30 (d, J=7.8 Hz, 2H); δ 6.94 (bs, 2H); GC-MS m/z 204 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067588B2
Source datasetuspto-grants-2011_11
ORD IDord-c02e39242dcd45e7a2a591a0202b05ee
Source noteuspto-grants-2011_11