HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-(Benzyloxy)-4-bromo-2-ethyl-5-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(Benzyloxy)-1-ethyl-4-methoxybenzene | HCID 22662099 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-(Benzyloxy)-4-bromo-2-ethyl-5-methoxybenzene | HCID 22662106 | — |
Reaction Steps
In a bromination reaction, the 3-benzyloxy-4-ethyl-1-methoxybenzene (3) is combined with N-bromosuccinimide (NBS) and silica gel 60 (EM Science, 480 Democrat Road, Gibbstown, N.J. 08027, an affiliate of Merck KGaA, Darmstadt, Germany) in a nonpolar solvent such as carbon tetrachloride at a temperature from about 0° C. to about room temperature. Preferably, the reaction is conducted at about room temperature. This reaction is allowed to stir, in the absence of light, to yield 5-benzyloxy-2-bromo-4-ethyl-1-methoxybenzene (4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06803470B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-5ee50cd272504f13b1988b21ab1465e4 |
| Source note | uspto-grants-2004_10 |