HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 929-53-3
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Product | 929-53-3 | HCID 11062440 | — |
| Product | 2,5-undecadiyn-1-ol | HCID 11116393 | — |
Reaction Steps
A solution of deca-1,4-diyne in THF was prepared following the method indicated in Example 1 and then an equivalent of ethylmagnesium bromide was added thereto at 0°. The mixture was kept at 60° for 45 min. After having added 1,2 equivalent of paraformaldehyde, the mixture was brought to reflux for 3 h. Once cooled, it was extracted with petroleum ether 80:100° and the organic phases were washed with water, then with an aqueous solution saturated with NaCl, dried and evaporated. The obtained residue was chromatographed on a column filled with silica, using as eluting agent a mixture of 1 to 10% of ethyl acetate in cyclohexane. Undeca-2,5-diyn-1-ol was thus obtained in 40% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05300716 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-f49d60ccd01e4267805676e1c0eb74fb |
| Source note | uspto-grants-1994_04 |