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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Tert-butyl but-3-en-1-yl(2-oxo-3-(triphenylphosphoranylidene)propyl)carbamate | HCID 118222052 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl N-but-3-enyl-N-(2-oxobut-3-enyl)carbamate | HCID 118222042 | 49.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09339510B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-87b3931401ce48a4bdaaab617862a1d4 |
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| Source note | uspto-grants-2016_05 |
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