HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 69585501, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1,1'-Azobis(cyclohexanecarbonitrile) | HCID 74978 | — |
| Reactant | HCID 69585958 | HCID 69585958 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 69585501 | HCID 69585501 | 100% |
Reaction Steps
In a 25 ml round-bottom flask, N-bromosuccinimide (236 mg, 1.3 mmol) and azobis(cyclohexanecarbonitrile) (33 mg, 0.14 mmol) were added to a solution of 3-methoxymethoxy-2-methyl-benzoic acid methyl ester (265 mg, 1.26 mmol) in carbon tetrachloride (6.5 ml). The reaction was heated to reflux with stirring for 3.5 hours. The volatiles were removed in vacuo and the residue purified by silica gel chromatography using a mixture of hexanes/ethyl acetate (9:1) as eluent, which afforded 364 mg (100%) of 2-bromomethyl-3-methoxymethoxy-benzoic acid methyl ester as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115624B1 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-61f1fdc99a9644039322e35dd4d32f5c |
| Source note | uspto-grants-2006_10 |