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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734635Generated: November 1, 2026

2,4,5-Trichloronitrobenzene → HCID 67654434, compound

https://huagongshe.com/reaction/1734635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,5-TrichloronitrobenzeneHCID 6983—
ReactantTriethylamineHCID 8471—
Reactantrac-(1R,2R,3S)-3-Amino-1,2-cyclopentanediolHCID 13497972—
Solventtert-ButanolHCID 6386—
ProductHCID 67654434HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534535
Source datasetuspto-grants-1996_07
ORD IDord-b5f0ef754d1349e7ba0e4a67efd0a6dc
Source noteuspto-grants-1996_07