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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994043Generated: October 30, 2026

4-Hydroxybenzoic acid hydrazide → HCID 136179690, compound

https://huagongshe.com/reaction/1994043

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic acid hydrazideHCID 1742—
Reactant2-Chloro-5-trifluoromethylphenyl isothiocyanateHCID 141005—
CatalystMercuric oxideHCID 30856—
SolventMethanolHCID 887—
ProductHCID 136179690HCID 13617969088.2%

Reaction Steps

Mercury (II) oxide yellow (1.82 g, 8.41 mmol) was suspended in ca. 50 mL of anhydrous methanol. 4-Hydroxybenzoic acid hydrazide (1.28 g, 8.41 mmol) was added to this bright-orange suspension, followed by 2-chloro-5-trifluoromethyl-phenylisothiocyanate (2.0 g, 8.41 mmol). The reaction mixture was brought to reflux and refluxed for 2 hours. The reaction mixture turned pitch-black in color and formed black precipitate. Then it was cooled down to ambient temperature and filtered through a short pad of Celite, then through a short pad of silica gel. Then methanol was removed in vacuo and the resulting grey solid was re-crystallized from ca. 20 mL of EtOAc. The formed white precipitate was filtered, washed with anhydrous Et2O and dried in vacuo to give the title product as a white solid (2.638 g). Yield 88.1%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652051B2
Source datasetuspto-grants-2010_01
ORD IDord-f2b850e2c5eb4e70bb8555474446a092
Source noteuspto-grants-2010_01