HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974402Generated: October 27, 2026
Hydrochloric Acid → N-[(2,4-difluorophenyl)methyl]-N-hexyl-2,2-dimethylpentanamide
https://huagongshe.com/reaction/974402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2-Dimethylvaleroyl chloride | HCID 519171 | — |
| Reactant | N-Hexyl-2,4-difluorobenzylamine | HCID 19986431 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[(2,4-difluorophenyl)methyl]-N-hexyl-2,2-dimethylpentanamide | HCID 19986408 | — |
Reaction Steps
22.7 g (0.10 mol) of N-hexyl-2,4-difluorobenzylamine and 24.3 g (0.24 mol) of triethylamine are dissolved in 150 ml of diethyl ether. A solution of 17.8 g (0.12 mol) of 2,2-dimethylpentanoyl chloride in 50 ml of diethyl ether is added dropwise at room temperature over the course of 30 minutes. The mixture is stirred for a further 18 hours at room temperature until the reaction is complete (GC check). For work-up, the resultant suspension is adjusted to pH 7 using 70 ml of 2N hydrochloric acid. Everything dissolves, and two phases form, which are separated. The organic phase is washed with 50 ml of water, dried using magnesium sulfate, filtered and evaporated on a vacuum rotary evaporator. 37.8 g of a pale yellow liquid, which is subjected to fractional distillation, are obtained. 21.4 g (63% of theory) of a colourless oil which boils at 126°-127° C. and 0.4 mbar are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05068371 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-fe2b8316ba6441fdaffddef32041f8b6 |
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| Source note | uspto-grants-1991_11 |
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