Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5558Generated: October 25, 2026

Furfural → 1-(Furan-2-yl)pentan-1-ol

https://huagongshe.com/reaction/5558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418682HCID 178418682—
SolventTetrahydrofuranHCID 8028—
Product1-(Furan-2-yl)pentan-1-olHCID 249285—

Reaction Steps

Freshly distilled furfural (233.5 g, 2.43 mol) was dissolved in 200 mL freshly distilled THF and added dropwise to a solution of butylmagnesium bromide (2.0 M in THF, 1460 mL, 2.92 mol) at 0° C. under dry nitrogen. After the addition was complete, the mixture was allowed to warm to room temperature overnight. The reaction was recooled to 0° C. and carefully poured into 2 L of cold sat. NH4Cl. The layers were separated, and the aqueous phase was extracted with ether. The combined organic layers were washed with saturated NaCl, dried over MgSO4, evaporated, and vacuum distilled to give 325.6 g (87%): bp 72°-73° C. (0.6 mmHg); 1H NMR (300 MHz, CDCl3) d 7.38 (1H, dd J=1 Hz), 6.33 (1H, m), 6.22 (1H, dd, J=3 Hz), 4.67 (1H, t, J=6 Hz), 2.9 (3H, m), 1.35 (4H, m), 0.90 (3H, t, J=7 Hz); mass spectrum (FAB): 170 (M+NH4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244910
Source datasetuspto-grants-1993_09
ORD IDord-6c6d592bcf1a42debe7854b152d5967a
Source noteuspto-grants-1993_09