HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl bromide → 4-(3-Chloropropoxy)-benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | 4-(3-Chloropropoxy)benzyl alcohol | HCID 22897496 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(3-Chloropropoxy)-benzyl bromide | HCID 21882276 | — |
Reaction Steps
A solution consisting of 4-(3-chloropropoxy)-benzyl alcohol No. 162 (10.6 g, 52.8 mmol) in dioxane (0.125 l) was cooled to 0° C. and treated with a dropwise addition of thionyl bromide (12.0 g, 58.0 mmol). After 10 minutes the reaction was complete. The dioxane was diluted with ethyl ether and washed with water, brine, and then dried over MgSO4. The material was concentrated down to yield 15 g of an oil: 1H NMR (DMSO) 7.36 (d, 2 H, J=8.8 Hz), 6.92 (d, 2 H, J=8.6 Hz), 4.68 (s, 2 H), 4.08 (t, 2 H, J=5.9 Hz), 3.77 (t, 2 H, J=6.4 Hz); MS (FAB) 266 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06924281B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-bd9d4db4d73548c3a39c7e8279000e13 |
| Source note | uspto-grants-2005_08 |