Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657060Generated: October 26, 2026

Hydrochloric Acid → 3,5-Di-tert-butyl-4-hydroxybenzohydrazide

https://huagongshe.com/reaction/1657060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1,1-Dimethylethyl 2-[3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoyl]hydrazine carboxylic acidHCID 18949819—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3,5-Di-tert-butyl-4-hydroxybenzohydrazideHCID 1042293466%

Reaction Steps

1,1-Dimethylethyl 2-[3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoyl]hydrazine carboxylic acid (4.0 g , 0.011 mole) in tetrahydrofuran (100 ml) is treated with a mixture of water (12 ml) and concentrated hydrochloric acid (30 ml). The resulting mixture is heated on a steam-bath. After 20 minutes the mixture is stripped of volatiles under reduced pressure. The residue is dissolved in water (100 ml) and treated with 1M NaOH until the solution is slightly basic. The product is extracted into ether (600 ml) and the organic layer is washed with saturated aqueous NaCl and dried over MgSO4. Filtration and concentration provides a solid which is recrystallized from isopropyl ether/hexane to yield 1.9 g (2.9 g theor., 66%) of 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoic acid, hydrazide, mp 187°-188° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256680
Source datasetuspto-grants-1993_10
ORD IDord-90a82b9aa7904dddbc6f6c57beff62cb
Source noteuspto-grants-1993_10