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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,5-Di-tert-butyl-4-hydroxybenzoic acid | HCID 15007 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9996322 | HCID 9996322 | 92.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05376670 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-eb006d40ddb448489b39cd7de2507a51 |
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| Source note | uspto-grants-1994_12 |
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