HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358731Generated: October 27, 2026
Hydrochloric Acid → HCID 20066743, compound
https://huagongshe.com/reaction/358731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Hexadecanamide, N,N-dimethyl- | HCID 19766 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20066743 | HCID 20066743 | 96.6% |
Reaction Steps
To a solution of n-butyl lithium (hexane, 44 mmol) in 120 mL of anhydrous tetrahydrofuran at 0° C., under nitrogen atmosphere it was added 6.2 mL (44 mmol) of diisopropylamine. After 5 min., 10 g (35 mmol) of N,N-dimethylhexadecanamide was added dropwise and the solution was stirred for 1 h at the same temperature. To the solution 3.7 mL (44 mmol) of allyl bromide were added and the mixture was stirred at room temperature for 12 h. Afterwards the solution was poured on water and the resulting mixture was acidified with 12 N HCl, and extracted twice with ethyl acetate. The organic phase was dried over anhydrous sodium sulfate and after evaporation of the solvent it was obtained 10.94 g of an oil that was purified by column chromatography (silica gel, hexane: ethyl acetate 15%). In that way, 10.2 g of a colorless oil was obtained (85% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04997843 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-fd72b1ba4c804c6e8707859de78dae7c |
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| Source note | uspto-grants-1991_03 |
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