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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915104Generated: 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/1915104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium NitrateHCID 24434—
Reactant4-(tert-Butyl)-2-(2-cyanopropan-2-yl)phenyl methyl carbonateHCID 59544146—
SolventDichloromethaneHCID 6344—
Product2-(1-Amino-2-methyl-1-oxopropan-2-yl)-4-tert-butyl-5-nitrophenyl methyl carbonateHCID 59544163—

Reaction Conditions

Temperature30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614325B2
Source datasetuspto-grants-2013_12
ORD IDord-33c5d71e248c4041871398dc799f9d90
Source noteuspto-grants-2013_12