HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518926Generated: October 26, 2026
Imidazole → 4-[(tert-butyldimethylsilyl)oxy]-N-phenylaniline
https://huagongshe.com/reaction/518926
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 4-Hydroxydiphenylamine | HCID 31208 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[(tert-butyldimethylsilyl)oxy]-N-phenylaniline | HCID 91741586 | — |
Reaction Steps
To a solution of 12 g of 4-anilinophenol (64.7 mmol) in 200 mL of acetonitrile there are added, at ambient temperature, 6.7 g of imidazole (97.05 mmol) and 11.7 g of tert-butyl(chloro)dimethylsilane (77.64 mmol). The batch is stirred at 70° C. for 4 hours. The reaction mixture is then poured into water and extracted with ether. The organic phase is then dried over magnesium sulphate, then filtered and evaporated to dryness. The crude product thereby obtained is then purified by chromatography over silica gel (petroleum ether/dichloromethane gradient). The title product is obtained in the form of a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115159B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-38cd0277e98c48ea9bd94c47b89a9275 |
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| Source note | uspto-grants-2015_08 |
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