HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168951Generated: October 29, 2026
tert-Butanol → tert-Butyl (5-methoxy-2-nitrophenyl)carbamate
https://huagongshe.com/reaction/2168951
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 5-Methoxy-2-nitrobenzoic acid | HCID 339209 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl (5-methoxy-2-nitrophenyl)carbamate | HCID 10199249 | — |
Reaction Steps
5-Methoxy-2-nitrobenzoic acid (10.30 g) was suspended in toluene (200 ml), triethylamine (9 ml) and diphenylphosphoryl azide (14 ml) were added dropwise at room temperature, and the mixture was stirred at 95° C. for 1.5 hr. Triethylamine (29 ml) and 2-methylpropan-2-ol (15 ml) were added, and the mixture was further stirred at 95° C. for 3 hr. The reaction mixture was concentrated under reduced pressure, and diluted with ethyl acetate. 0.5M Hydrochloric acid (200 ml) was added, and the mixture was filtered through celite. The organic layer of the filtrate was collected, washed with saturated aqueous sodium hydrogen carbonate, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, and a fraction eluted with ethyl acetate-hexane (5:95-1:1) was concentrated under reduced pressure to give the object product (13.28 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045436B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-db6c8d2de4384f06b1ada91161f5ff6d |
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| Source note | uspto-grants-2015_06 |
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