HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112048Generated: November 2, 2026
Phenylacetyl chloride → HCID 5152095, compound
https://huagongshe.com/reaction/2112048
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | 1-Heptanamine | HCID 8127 | — |
| Reactant | Benzyldiisopropylamine | HCID 4578032 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 5152095 | HCID 5152095 | 43.7% |
Reaction Steps
Heptan-1-amine (1 g, 8.679 mmol) was dissolved in dry THF under N2 and polymer supported N-benzyl-N,N-diisopropylamine (4.955 g, 26.038 mmol) was added. The mixture was stirred for 30 min and cooled to 0 degrees and phenylacetyl chloride (1.610 g, 10.415 mmol) was added. The solution was stirred overnight at room temperature. The excess of phenylacetyl chloride was removed by filtering the mixture through an NH2 cartridge. The solvent was removed by evaporation. The crude was purified by preparative HPLC (started with isocratic acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min). The product containing fractions were pooled and the acetonitrile was removed by evaporation. EtOAc (10 ml) was added and the organic phase was washed with two portions of brine and dried (MgSO4) and the solvent was removed by evaporation to give 0.886 g of N-heptyl-2-phenylacetamide (yield 43.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07521461B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-06b8575ff03e49cda68866aa9a8ebf56 |
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| Source note | uspto-grants-2009_04 |
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