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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492992Generated: October 30, 2026

3,5-Di-tert-butyl-4-hydroxybenzoic acid → HCID 9996322, compound

https://huagongshe.com/reaction/1492992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 15007—
ReactantOxalyl chlorideHCID 65578—
ReactantThiosemicarbazideHCID 2723789—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9996322HCID 999632292.2%

Reaction Steps

Oxalyl chloride (11.5 g, 0.091 mole) is added dropwise to a stirred 0° C. solution of 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoic acid (15.0 g, 0.059 mole) in methylene chloride (120 ml) and N,N-dimethylformamide (0.5 ml). After one hour, the solvent is removed in vacuo. The residue is dissolved in tetrahydrofuran (70 ml) and added dropwise to a stirred 0° C. suspension of thiosemicarbazide (10.9 g, 0.120 mole) in tetrahydrofuran (300 ml). After the addition is complete the mixture is allowed to warm to room temperature and stir 18 hours. The mixture is concentrated in vacuo and the residue filtered through a plug of flash silica gel using a 1:1 ethyl acetate/heptane mixture as eluent. Concentration and trituration with 1:1 isopropyl ether/hexane yielded 17.6 g (19.4 g theor., 91%) of 2-[3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoyl]hydrazinecarbothioamide, mp 210°-211° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05376670
Source datasetuspto-grants-1994_12
ORD IDord-eb006d40ddb448489b39cd7de2507a51
Source noteuspto-grants-1994_12