HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617299Generated: October 25, 2026
Sulfuric Acid → 2-(1-Amino-2-methyl-1-oxopropan-2-yl)-4-tert-butyl-5-nitrophenyl methyl carbonate
https://huagongshe.com/reaction/1617299
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 4-(tert-Butyl)-2-(2-cyanopropan-2-yl)phenyl methyl carbonate | HCID 59544146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-Amino-2-methyl-1-oxopropan-2-yl)-4-tert-butyl-5-nitrophenyl methyl carbonate | HCID 59544163 | — |
Reaction Steps
To a stirred mixture of compound 16 (10.0 g, 36.3 mmol) and KNO3 (5.51 g, 54.5 mmol) in DCM (1000 mL) was added dropwise 98% H2SO4 (145.4 g, 1.45 mol) at 0° C. The mixture was stirred at 30° C. for 4 days. The H2SO4 layer was then separated and poured into ice-water (50 g) and then extracted with DCM (100 mL×3). The combined organic layers were washed with water, aqueous NaHCO3 solution and brine, then dried over MgSO4 and concentrated in vacuo. The residue was purified via column chromatography on silica gel (Petroleum ether/EtOAc 20:1→10:1→5:1→3:1) to give compound 17 as a yellow solid. 1H NMR (CDCl3; 400 MHz) δ 8.05 (s), δ 7.74 (s), δ 7.61 (s), δ 7.32 (s), δ 5.32 (s), δ 3.91 (s), δ 3.92 (s), δ 1.62 (s), δ 1.59 (s), δ 1.42 (s), δ 1.38 (s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765957B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-b5f8b5c8f20d40f4bce4616f52634251 |
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| Source note | uspto-grants-2014_07 |
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