HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363285Generated: November 3, 2026
2-Chloropropane → 4-ISOPROPYLFURAN-2-CARBALDEHYDE
https://huagongshe.com/reaction/1363285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloropropane | HCID 6361 | — |
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 4-ISOPROPYLFURAN-2-CARBALDEHYDE | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07884124B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-f8447c41b962472ea717289da12d6718 |
|---|
| Source note | uspto-grants-2011_02 |
|---|