HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 18436659, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | HCID 18436663 | HCID 18436663 | — |
| Product | HCID 18436659 | HCID 18436659 | — |
Reaction Steps
tert-Butyl-{2-[2-(2-chloro-ethoxy)-ethoxy]-ethoxy}-dimethyl-silane was converted to the corresponding iodide by refluxing with 5 equiv of NaI in 2-butanone for 6 h. This was then alkynylated and deprotected by the same process described above to provide E-5-Ethoxy-pent-4-en-1-ol: 1H NMR (500 MHz) 4.02 (q, J=6.8, 2H, H2C(5″)); 3.74–3.70 (m, 2 H, HCO); 3.68–3.66 (m, 2H, HCO); 3.64–3.60 (m, 4H, HCO); 3.54 (t, J=7.3, 2H, H2CO)); 2.49 (t, J=6.3, 1H, OH); 2.41 (t, J 7.3, 2H, H2CO); 1.33 (t, J=7.3, 3H, H3C(6″)); 13C NMR (100 (M+NH4); 186.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186709B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-023792da668641419d66648e0fa4201c |
| Source note | uspto-grants-2007_03 |