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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-methylbutaneHCID 7891—
ReactantHCID 178418439HCID 178418439—
SolventWaterHCID 962—
ProductThiophene, 2-isopentyl-HCID 11789988.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597832
Source datasetuspto-grants-1997_01
ORD IDord-524b9e03480a4f4b83c07433c4943f12
Source noteuspto-grants-1997_01