HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodophenol → HCID 18442679, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodophenol | HCID 10894 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 86602295 | HCID 86602295 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18442679 | HCID 18442679 | — |
Reaction Steps
2 g of methanesulfonic acid 3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propyl ester, 1.14 g of 4-iodophenol and 1.96 g of potassium carbonate are stirred for 24 hours at 50° C. in 20 ml of dimethylformamide. The reaction mixture is poured onto water and extracted with ethyl acetate. The organic phase is washed with water and potassium carbonate solution and concentrated. Purification over silica gel yields 1,3-dichloro-5-(3,3-dichloro-allyloxy)-2-[3-(4-iodo-phenoxy)-propoxy]-benzene. 1H-NMR (CDCl3) 300 MHz: 2.28 (m, 2H), 4.13 (t, 2H), 4.22 (t, 2H), 4.58 (d, 2H), 6.10 (t, 1H), 6.71 (d, 2H), 6.81 (s, 2H), 7.55 (d, 2H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07608631B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-b6e400610f7c4b0babeb5ae9fa5ff4ec |
| Source note | uspto-grants-2009_10 |