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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898775Generated: November 1, 2026

Iodoethane → 5-Ethoxy-1-pentanol

https://huagongshe.com/reaction/1898775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant1,5-PentanediolHCID 8105—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Ethoxy-1-pentanolHCID 1302793071.1%

Reaction Steps

NaH (4.2 g, 0.11 mol) was washed with hexane and then suspended in dry THF (400 mL). Pentane-1,5-diol (10.4 g, 0.1 mol) in THF (50 mL) was added and stirred for 1 h at room temperature. Iodoethane (17.2 g, 0.11 mol) in THF (50 mL) was added and the mixture was refluxed for 48 h. After evaporation of the solvent, the residue was dissolved in EtOAc (300 mL). The organic phase was washed with water (2×50 mL ), brine (50 mL ), and dried (Na2SO4). The residue was purified by column chromatography on alumina with 10% 2-propanol in hexane, and then Kugelrohr distillation to give the title product (2) (9.4 g, 71%); bp 45°-46° C./0.005 torr; IR(neat): 3400 (broad) and 1115 cm-1 ; 1H NMR: 1.22 (t, 3H, J=6.8 Hz), 1.42 (m, 2H), 1.56 (m, 4H), 3.43 (t, 4H, J=5.8 Hz), 3.48 (q, 2H, J=6.8 Hz), and 3.58 ppm (b s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571689
Source datasetuspto-grants-1996_11
ORD IDord-8a19eef396934ad7aea4941498d19ea2
Source noteuspto-grants-1996_11