Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | 4-Bromo-2,6-xylidine | HCID 90549 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 3601868 | HCID 3601868 | 50% |
Reaction Steps
4-Bromo-2,6-dimethyl-aniline (0.50 g) and hexanoyl chloride (0.45 mL) were dissolved in acetonitrile (4 mL) and heated to 150° C. for 10 minutes in a sealed microwave process vial. The reaction mixture was concentrated in vacuo and purified by flash chromatography to furnish 0.37 g (50% yield) of the title compound as a white solid. LC-MS (m/z) 299 (MH+); tR=3.09, (UV, ELSD) 100%, 99%. 1H NMR (500 MHz, CDCl3): 0.93 (t, 3H), 1.39 (m, 4H), 1.76 (qui, 2H), 2.20 (s, 6H), 2.40 (t, 2H), 6.57 (b, 1H), 7.23 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601870B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-a442f313bcc24a4f8d536d78c98b142d |
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| Source note | uspto-grants-2009_10 |
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