Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-(diethoxyphosphoryl)butanoate | HCID 229053 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 2-methylidenebutanoate | HCID 291416 | 87% |
Reaction Steps
A mixture of 5.0 g (0.019 mol) of triethyl 2-phosphonobutyrate, 5.5 g (0.039 mol) of K2CO3, 6.2 g (0.076 mol) of 37% aqueous formaldehyde solution, and 15 ml of water was heated to about 80° C. for about 45 min. After cooling to RT, 75 ml of ether was added and the organic layer was separated, washed with brine (1×20 ml), dried (MgSO4), and filtered. The ether was carefully removed by distillation, leaving behind 2.1 g (87%) of the title compound as a clear oil which was used directly without further purification. 1H NMR (CDCl3): δ 1.01 (3H, t, J=7), 1.24 (3H, t, J=7), 2.26 (2H, q, J=7) 4.14 (2H, q, J=7), 5.45 (1H, s), 6.06 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686434 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-be455c16421a4598906c91b036d0ece9 |
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| Source note | uspto-grants-1997_11 |
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