HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-(Bromomethyl)-2,5-dichlorothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,5-Dichloro-3-methylthiophene | HCID 268910 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-(Bromomethyl)-2,5-dichlorothiophene | HCID 23434082 | 91.1% |
Reaction Steps
To a stirred solution of 2,5-dichloro-3-methylthiophene (25.8 g, 154 mmol) in carbon tetrachloride (47 mL) was added N-bromosuccinimide (27.5 g, 154 mmol) and benzoyl peroxide (310 mg, 1.28 mmol). The mixture was heated at reflux temperature for 8 hours. After cooling, the insolubles were filtered off. The filtrate was washed with aqueous sodium sulfite solution, dried over MgSO4, and concentrated in vacuo. The residue was fractionally distilled under reduced pressure (bp 80° C., 0.5 mmHg) to give the subtitle compound (34.5 g, 91% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048880 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-0bdfe2261e10431a8fe862dfc87a5c9b |
| Source note | uspto-grants-2000_04 |