HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,5-Trichloronitrobenzene → HCID 67654434, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,5-Trichloronitrobenzene | HCID 6983 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | rac-(1R,2R,3S)-3-Amino-1,2-cyclopentanediol | HCID 13497972 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 67654434 | HCID 67654434 | — |
Reaction Steps
(±)-(1R*, 2S*, 3R*)-3-Amino-1,2-cyclopentanediol (7.10 g, 50.0 mmol), 1,2,4-trichloro-5-nitrobenzene (11.67 g, 50.0 mmol as 97%, Aldrich), triethylamine (10 mL) and t-butanol (50 mL) were refluxed under nitrogen for 7 hours. Volatiles were removed in vacuo and the black residue chromatographed on silica gel. Title compound was eluted with methanol:chloroform/1:24 as an orange solid (6.45 g, 42%). Crystallization of such a sample from ethanol-water gave title compound as yellow needles, m.p. 137°-140° C.; 1H-NMR (DMSO-d6)δ: 8.26 and 7.49 (both s, 1 each, 2 aromatic CH), 8.06 (d, J=7.0 Hz, 1, NH), 5.04 (d, J=6.1 Hz, 1, OH), 4.65 (d, J=4.1 Hz, 1, OH), 4.0-3.7 (m, 3, 2 OCH and NCH), 2.2-2.21, 2.0-1.8, 1.7 -1.3 (all m, 4, 4 CH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534535 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-b5f0ef754d1349e7ba0e4a67efd0a6dc |
| Source note | uspto-grants-1996_07 |