HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → (2-Bromo-5-chlorothiophen-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | (2-Bromothiophen-3-yl)methanol | HCID 12479010 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Bromo-5-chlorothiophen-3-yl)methanol | HCID 57900970 | — |
Reaction Steps
To a solution of 2-bromo-3-hydroxymethylthiophene from Example 1, Step 1 (13.0 g, 67.3 mmol) in THF (100 mL) and water (10 mL) was added N-chlorosuccinimide (9.88 g, 74.0 mmol) and the mixture was stirred at r.t. for 5 h and concentrated in vacuo. The residue was worked up as above to afford the desired product. The crude product was used directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969394B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-127fbcdd4fee4fa897c12acf1cd519ff |
| Source note | uspto-grants-2015_03 |