HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 5-(Bromomethyl)thiophene-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-(Hydroxymethyl)thiophene-2-carbonitrile | HCID 10606813 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Bromomethyl)thiophene-2-carbonitrile | HCID 10560016 | 75% |
Reaction Steps
To a solution of 2-cyano-5-(hydroxymethyl)thiophene (6.0 g, 43 mmol) in THF (50 mL) was added triphenylphosphine (15.7 g, 47 mmol) and carbon tetrabromide (12.3 g, 47 mmol). After stirring overnight under nitrogen atmosphere at room temperature, the solvent was removed in vacuo and the residue was dissolved in chloroform, then adsorbed onto silica gel and loaded onto a silica gel column. The product was eluted using an ethyl acetate/hexanes gradient. Fractions containing pure product (as judged by TLC) were pooled and concentrated in vacuo to give 6.5 g (75%) of 2-cyano-5-(bromomethyl)thiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726159 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-69104add2a2849aba17decff43b8a344 |
| Source note | uspto-grants-1998_03 |