HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 4-Ethylhex-2-yn-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl but-2-ynoate | HCID 141019 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Product | 4-Ethylhex-2-yn-4-ol | HCID 19367730 | — |
Reaction Steps
A solution of methyl 2-butynoate (1.5 g) in ether (50 ml) was cooled to 0°, treated with ethyl magnesium bromide (21 ml of a 3M solution in ether) and stirred at room temperature for 4 hours. The mixture was then cooled to 0° and treated with saturated ammonium chloride solution, whereafter the product was extracted into ether and the title compound (1.2 g) was isolated by chromatography. IR (CCl4) νmax 2200 (C≡C), 3450 cm-1 (OH); NMR (CCl4) δ 1.83 (s, H3C--C≡), 2.3 (s), 1.36-1.6 (m, CH2CH3), 0.93 (t, CH3CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05872140 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-f9ef5d397b054e2b896dbc3f21cf77d0 |
| Source note | uspto-grants-1999_02 |