HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235093Generated: October 26, 2026
1-Bromo-3-methylbutane → Thiophene, 2-isopentyl-
https://huagongshe.com/reaction/235093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-methylbutane | HCID 7891 | — |
| Reactant | HCID 178418439 | HCID 178418439 | — |
| Solvent | Water | HCID 962 | — |
| Product | Thiophene, 2-isopentyl- | HCID 117899 | 88.1% |
Reaction Steps
Isopentyl bromide (Aldrich, 8 g, 53mmol) was added to 53 mL of an ice-cooled solution of lithiothiophene (1.0M in THF, 53 mmol). The reaction was stirred at 0° C. for 2 hours, at room temperature for 16 hours, and poured into water, then the mixture was extracted with hexane. The organic layer was dried and concentrated, and the residue was purified by column chromatography on silica gel, eluting with hexane, to give 7.2 g (88% yield) of the title compound as a colorless oil. NMR (CDCl3) δ:7.10 (dd, J=1, 6 Hz, 1H), 6.90 (dd, J=4, 6 Hz, 1H), 6.78 (dd, J=1, 4 Hz, 1H), 2.84 (t, J=8 Hz, 2H), 1.7-1.5 (m, 3H), 0.94 (d, J=6 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05597832 |
|---|
| Source dataset | uspto-grants-1997_01 |
|---|
| ORD ID | ord-524b9e03480a4f4b83c07433c4943f12 |
|---|
| Source note | uspto-grants-1997_01 |
|---|