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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574748Generated: October 30, 2026

Dimethylformamide → HCID 86676971, compound

https://huagongshe.com/reaction/574748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSolketalHCID 7528—
Reactant1-BromohexadecaneHCID 8213—
ReactantSodium hydrideHCID 24758—
ProductHCID 86676971HCID 8667697157%

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): 8 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 numberUS09034923B2
Source datasetuspto-grants-2015_05
ORD IDord-40c40e4335dd4cb39e53d2ad01d0611a
Source noteuspto-grants-2015_05