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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054326Generated: October 26, 2026

3-Chlorobenzaldehyde → HCID 74763783, compound

https://huagongshe.com/reaction/1054326

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorobenzaldehydeHCID 11477—
Reactant2-Amino-5-chloropyridineHCID 66174—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantIsocyanocyclopropaneHCID 2758008—
SolventMethanolHCID 887—
ProductHCID 74763783HCID 7476378318.2%

Reaction Steps

5-chloropyridin-2-amine (100 mg, 778 μmol, Eq: 1.00), 3-chlorobenzaldehyde (115 mg, 93.0 μl, 817 μmol, Eq: 1.05) and p-toluenesulfonic acid monohydrate (44.4 mg, 233 μmol, Eq: 0.3) were dissolved in MeOH (1.00 mL) and the intensive yellow solution was stirred for 10 min. To this yellow solution was added dropwise isocyanocyclopropane (52.2 mg, 47.4 μL, 778 μmol, Eq: 1.00) and the corresponding yellow solution was stirred for 2 h. The solvent was removed and the dark red oil was purified twice by flash column chromatography (ethyl acetate in hexanes) to give the product as yellow solid (45 mg, 18.2%). LC/MS (acid polar): 318.1 [M+H]+; 1H-NMR (CDCl3): δ 8.50 (s, 1H), 8.21 (s, 1H), 8.14 (d, 1H), 7.58 (d, 1H), 7.49 (t, 1H), 7.38 (d, 1H), 7.28 (d, 1H), 5.44 (s, 1H), 2.70 (m, 1H), 0.46-0.39 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394304B2
Source datasetuspto-grants-2016_07
ORD IDord-d91c3aad364748d1bede9c65528fd0ba
Source noteuspto-grants-2016_07