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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778606Generated: November 2, 2026

Potassium Carbonate → tert-Butyl 3-oxocyclobutylcarbamate

https://huagongshe.com/reaction/1778606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-butyl N-(3-methylidenecyclobutyl)carbamateHCID 28875369—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-oxocyclobutylcarbamateHCID 23374584177.6%

Reaction Steps

To a vigorously stirring solution of N-Boc-3-methylene-cyclobutanamine (9.8 g, 53.5 mmol) in DCM (160 mL) and H2O (160 mL) was added K2CO3 (3 g, 21.7 mmol), followed by NaClO4 (35 g, 163.5 mmol), tetrabutylammonium chloride (0.2 g, 0.72 mmol) and RuCl3 (0.6 g, 7.6 mmol). During the course of the reaction, the organic solution turned dark brown, the catalyst turned black, while the upper aqueous layer turned white. The reaction was monitored by TLC, and upon completion, the reaction mixture was filtered through a pad of celite. The filtrates were transferred to a separatory funnel, and the aqueous layer was extracted with DCM (2×50 mL). The combined organic layers were washed with 5% NaHCO3 (2×30 mL), brine (30 mL), dried over Na2SO4, filtered and evaporated to dryness to yield a crude, which was purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-60%) to yield the desired N-Boc-3-amino-cyclobutanone (7.13 g, 38.53 mmol, 72% yield): NMR (250 MHz, CDCl3) δ 4.88 (bs, 1 H), 4.13-4.29 (m, 1 H), 3.23-3.41 (m, 2 H), 2.9-3.05 (m, 2 H), 1.39 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266919B2
Source datasetuspto-grants-2016_02
ORD IDord-40675c9ba0c24977ac7bc24204c11fb6
Source noteuspto-grants-2016_02