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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363285Generated: November 3, 2026

2-Chloropropane → 4-ISOPROPYLFURAN-2-CARBALDEHYDE

https://huagongshe.com/reaction/1363285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropropaneHCID 6361—
ReactantFurfuralHCID 7362—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
Product4-ISOPROPYLFURAN-2-CARBALDEHYDEHCID 12258806—

Reaction Steps

To a suspension containing aluminium chloride (24 g, 180 mmol) in 100 mL of CS2 was added 2-furaldehyde (9.8 mL, 156 mmol). To this mixture was added dropwise isopropyl chloride (14.3 mL, 156 mmol), and the resulting mixture stirred at rt for 24 h. The dark mixture was carefully poured into a vigorously stirred 250 g of ice, and then extracted with ether (5×100 mL). The combined organic layers were washed with water, brine, dried (Na2SO4), filtered through a pad of silica gel, and concentrated. The residue was purified by flash chromatography (0-5% EtOAc in heptane) to give 4-isopropylfuran-2-carbaldehyde as an orange oil: Yield 3.5 g (16%). 1H NMR (400 MHz, CDCl3) δ ppm 1.25 (d, J=6.88 Hz, 6H), 2.80-2.91 (m, 1H), 7.16-7.18 (m, 1H), 7.47 (q, J=0.91 Hz, 1H), 9.61 (d, J=0.59 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884124B2
Source datasetuspto-grants-2011_02
ORD IDord-f8447c41b962472ea717289da12d6718
Source noteuspto-grants-2011_02