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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Solketal | HCID 7528 | — |
| Reactant | 1-Bromohexadecane | HCID 8213 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[(Hexadecyloxy)methyl]-2,2-dimethyl-1,3-dioxolane | HCID 13916251 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993623B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-6d3388d808dc4316aa43f8dd73e29865 |
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| Source note | uspto-grants-2015_03 |
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