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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523626Generated: October 31, 2026

Formaldehyde → tert-butyl N-but-3-enyl-N-(2-oxobut-3-enyl)carbamate

https://huagongshe.com/reaction/523626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTert-butyl but-3-en-1-yl(2-oxo-3-(triphenylphosphoranylidene)propyl)carbamateHCID 118222052—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-but-3-enyl-N-(2-oxobut-3-enyl)carbamateHCID 11822204249.2%

Reaction Conditions

Temperature18 °C

Reaction Steps

To a mixture of tert-butyl N-but-3-enyl-N-[2-oxo-3-(triphenyl-phosphanylidene) propyl]carbamate (5.80 g, 11.90 mmol, 1.00 Eq) in THF (30 mL), was added HCHO (96.58 g, 1.19 mol, 100.00 Eq) in one portion at 18° C. The mixture was stirred at 18° C. for 15 hr. TLC showed the reaction was completed. The mixture was extracted with PE (100 mL*3). The combined organic phase was washed with saturated brine (200 mL*2), dried with anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by silica gel chromatography (PE/EA=50/1, 40/1) to afford tert-butyl N-but-3-enyl-N-(2-oxobut-3-enyl)carbamate (1.40 g, 5.85 mmol, 49.16% yield) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339510B2
Source datasetuspto-grants-2016_05
ORD IDord-87b3931401ce48a4bdaaab617862a1d4
Source noteuspto-grants-2016_05