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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881581Generated: November 3, 2026

Solketal → 4-[(Hexadecyloxy)methyl]-2,2-dimethyl-1,3-dioxolane

https://huagongshe.com/reaction/881581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSolketalHCID 7528—
Reactant1-BromohexadecaneHCID 8213—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product4-[(Hexadecyloxy)methyl]-2,2-dimethyl-1,3-dioxolaneHCID 1391625157%

Reaction Steps

To NaH (1.85 g, 60% dispersed in mineral oil) under argon was added anhydrous N,N-dimethylformamide (DMF, 30 mL) at RT. Solketal (2.20 g, 16.7 mmol) in 10 mL anhydrous DMF was then added dropwise with constant stirring. 1-Bromohexadecane (5.10 g, 16.7 mmol), dissolved in anhydrous DMF (20 mL) was then added to the reaction mixture dropwise and stirred for 72 hours. The reaction was quenched by adding about 5 mL of methanol. It was then poured into cold ice water (100 mL) and extracted with hexane (100 mL, 3×). The solvent was removed under reduced pressure and the residue chromatographed on silica gel using hexane-dichloromethane to obtain 1a (3.363 g, 57% yield); 1H NMR (in CDCl3): δ in ppm 0.83-0.86 (3H, t, J=6.5 Hz), 1.22 (26H, m), 1.33 (3H, s), 1.39 (3H, s), 1.52-1.55 (2H, m), 3.37-3.48 (4H, m), 3.68-3.71 (1H, t, J=6.5 Hz), 4.01-4.03 (1H, t, J=6.5 Hz), 4.20-4.25 (1H, quintet, J=6.0 Hz); 13C NMR (in CDCl3): δ in ppm 14.3, 22.9, 25.6, 26.2, 27.0, 29.6, 29.7, 29.8, 29.9, 32.1, 67.1, 72.0, 72.1, 74.9, 109.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993623B2
Source datasetuspto-grants-2015_03
ORD IDord-6d3388d808dc4316aa43f8dd73e29865
Source noteuspto-grants-2015_03