HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493034Generated: October 30, 2026
Guanidine Hydrochloride → HCID 178440701, compound
https://huagongshe.com/reaction/1493034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 136403400 | HCID 136403400 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178440701 | HCID 178440701 | 46.5% |
Reaction Steps
Sodium (0.68 g, 29.7 mmol) is dissolved in 40 ml of t-butanol under N2 atmosphere. Guanidine hydrochloride (3.31 g, 34.65 mmol) is added to the sodium t-butoxide solution and stirred at room temperature for 0.5 hour. 2,6-Bis(1,1-dimethylethyl)-4-[5-(methylsulfonyl)-1,3,4-oxadiazole-2-yl]-phenol (3.50 g, 9.93 mmol) is added and the reaction is warmed at reflux overnight. The cool reaction mixture is concentrated in vacuo and is recrystallized from methanol-water. The solid is dissolved in diethyl ether and treated with ethereal HCl and the precipitate is collected and recrystallized from ethanol-ether to give 1.53 g (3.29 g theor., 46%) of N-[5-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-1,3,4-oxadiazole-2-yl]-guanidine, monochloride as a white solid: mp 223°-224° 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-8769b6551ed142149c95b0715f08410c |
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| Source note | uspto-grants-1994_12 |
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