HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165141Generated: November 2, 2026
Sodium cyanoborohydride → HCID 19862543, compound
https://huagongshe.com/reaction/1165141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 135973970 | HCID 135973970 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19862543 | HCID 19862543 | — |
Reaction Steps
0.9 g of 1-(4-hydroxy-3,5-di-tert.-butylbenzylideneamino)imidazole are suspended in 10 ml of glacial acetic acid and treated with 1.61 g of sodium cyanoborohydride, whereby a solution results. The solution is stirred at room temperature overnight and then evaporated in a vacuum. The residue is treated with 10 ml of water, neutralized (pH=7) with ice-cold saturated sodium bicarbonate solution and extracted three times with 30 ml of methylene chloride each time. The combined organic phases are dried over sodium sulfate, filtered and evaporated in a vacuum. The residue is crystallized with ehter. The product is removed by filtration and reprecipitated from ethanol/water. There is obtained 1-(4-hydroxy-3,5-di-tert.-butylbenzylamino)imidazole of m.p. 171°-174°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04908363 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-42081a6a0aab4457801a1309febb7be1 |
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| Source note | uspto-grants-1990_03 |
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