HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl bromide → 1-(Bromomethyl)-4-(2-chloroethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | [4-(2-Chloroethoxy)phenyl]methanol | HCID 21882321 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(Bromomethyl)-4-(2-chloroethoxy)benzene | HCID 21882252 | 58% |
Reaction Steps
To 4-(2-Chloroethoxy)benzylalcohol CAS No. [111728-87-1] (6.4 g, 34.31 mmol) in dioxane (100 mL) at 0° C. was added slowly thionylbromide (7.13 g, 34.31 mmol). The reaction was run at 0° C. after 5 min. The reaction mixture was diluted with ether (200 mL) and washed with H2O (1×30 mL) then NaHCO3 (2×25 mL), and brine (30 mL). The organic extract was dried over MgSO4 and concentrated. The crude product was purified by silica gel chromatography (15% EtOAc/Hex) to yield 5.0 g (58%) of the desired product. Mp=64-66° C.; 1H NMR (DMSO) 7.37 (d, 2H, J=8.8 Hz), 6.93 (d, 2H, J=8.8 Hz), 4.68 (s, 2H), 4.24 (t, 2H, J=5.05 Hz), 3.93 (t, 2H, J=5.27 Hz); MS eI m/z 248 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07247624B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-ec39fe80c2af443b8d9fe4f54bd34bae |
| Source note | uspto-grants-2007_07 |