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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713147Generated: October 30, 2026

tert-butyl N-but-3-enyl-N-(2-oxobut-3-enyl)carbamate → tert-Butyl 3-oxo-2,3,6,7-tetrahydro-1H-azepine-1-carboxylate

https://huagongshe.com/reaction/713147

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-but-3-enyl-N-(2-oxobut-3-enyl)carbamateHCID 118222042—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-oxo-2,3,6,7-tetrahydro-1H-azepine-1-carboxylateHCID 7546489664.17%

Reaction Conditions

Temperature18 °C

Reaction Steps

To a mixture of tert-butyl N-but-3-enyl-N-(2-oxobut-3-enyl)carbamate (1.50 g, 6.27 mmol, 1.00 Eq) in DCM (250 mL), was added Zhan catalyst 1B (150.00 mg, 204.43 umol, 0.03 Eq) in one portion at 18° C. under N2. The mixture was stirred at 18° C. for 10 hr. TLC showed the reaction was completed. The mixture was concentrated in vacuum. The residue was purified by silica gel chromatography (PE/EA=30/1, 20/1) to afford tert-butyl 6-oxo-3,7-dihydro-2H-azepine-1-carboxylate (850.00 mg, 4.02 mmol, 64.17% yield) as yellow solid. 1H NMR (400 MHz, CHLOROFORM-d) 6.36-6.64 (m, 1H), 5.88-6.14 (m, 1H), 4.23-4.35 (m, 1H), 4.16 (s, 1H), 3.51-3.68 (m, 2H), 2.62-2.78 (m, 2H), 1.46 (d, J=17.32 Hz, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181288B2
Source datasetuspto-grants-2015_11
ORD IDord-4fdd961cd2f44e58a61b6904cce0e163
Source noteuspto-grants-2015_11