HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323023Generated: October 29, 2026
Imidazole → 2-[(Tert-butyldimethylsilyl)oxy]-4-nitroaniline
https://huagongshe.com/reaction/323023
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 2-Amino-5-Nitrophenol | HCID 4984721 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[(Tert-butyldimethylsilyl)oxy]-4-nitroaniline | HCID 15485710 | 98% |
Reaction Steps
To a solution of 2-amino-5-nitrophenol (1 g, 6.49 mmol) and imidazole (0.88 g, 12.3 mmol) in DMF (15 mL), tert-butyldimethylsilyl chloride (11.2 mL, 64.9 mmol) was added. The resulting mixture was allowed to stir at 23° C. for 48 hours. The reaction mixture was partitioned between 0.1% HCl and ethyl acetate. The combined organic phase was washed with brine, dried over MgSO4 and filtered. Removal of solvent at reduced pressure and chromatography of the resulting oil on silica gel (hexane:ethyl acetate; 5:1) gave the titled compound (1.7 g, 98%). 1H NMR (CDCl3): d 7.78 (dd, 1H, J=6.7 Hz and J=2.7 Hz), 7.61 (d, 1H, J=2.7 Hz), 6.7 (d, 1H, J=8.8 Hz), 1.0 (s, 9H), 0.28 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211373B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-2ab9f5acaee64421a9fbc9b29cfdf890 |
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| Source note | uspto-grants-2001_04 |
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