HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820128Generated: October 30, 2026
Cyclohexylpropionyl chloride → HCID 68712047, compound
https://huagongshe.com/reaction/1820128
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexylpropionyl chloride | HCID 2734098 | — |
| Reactant | 2-bromo-4-nitro-6-(trifluoromethyl)aniline | HCID 11471654 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68712047 | HCID 68712047 | 33% |
Reaction Steps
2-Bromo-4-nitro-6-trifluoromethyl-phenylamine (2.0 g) and cyclohexylpropionyl chloride (1.30 mL) were mixed in acetonitrile (10 mL) and heated to 150° C. for 10 minutes in a sealed microwave process vial. The reaction was cooled to 0° C., the product filtered off and washed with cold acetonitrile (50 mL) affording 0.97 g (33% yield) of the title compound as a yellow solid. The crude product was used without further purification. LC-MS (m/z) 424 (MH+); tR=3.53, (UV, ELSD) 95%, 99%. 1H NMR (500 MHz, DMSO-d6): 0.88 (m, 2H), 1.17 (m, 3H), 1.28 (m, 1H), 1.51 (m, 2H), 1.68 (m, 5H), 2.38 (t, 2H), 8.45 (d, 1H), 8.82 (d, 1H), 10.17 (s, 1H).
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-b71213bd48a7486cbe1c3c592ceaa3e0 |
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| Source note | uspto-grants-2009_10 |
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