Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840290Generated: October 31, 2026

Pyridine → HCID 870083, compound

https://huagongshe.com/reaction/1840290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-bromobutanimideHCID 67184—
ReactantN-[(4-fluorophenyl)methylidene]hydroxylamineHCID 68017—
ReactantHCID 260134HCID 260134—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 870083HCID 87008347%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1.05 g of 4-fluorobenzaldoxime (Beil. 7, I 132d, II 177d, III 863c) in 15 mL of chloroform were added 1.35 g of N-bromosuccinimide (NBS) and 0.04 mL of pyridine; the resulting mixture was stirred at r.t for 4 h under nitrogen atmosphere. After cooling at 0° C., 1.75 g of methyl β-pyrrolidinoacrylate (prepared as described in U.S. Pat. No. 4,144,047) and 1.26 mL of triethylamine were added and the suspension was stirred at r.t. for 18 h. The reaction mixture was diluted with 20 mL of 2 N hydrochloric acid, 20 mL of water; the organic layer was separated, washed again with 2 N hydrochloric acid and water, dried (sodium sulphate), and evaporated to dryness in vacuo. The crude was purified by flash chromatography (toluene-dichloromethane 1:9) to afford the title compound (47%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680319B2
Source datasetuspto-grants-2004_01
ORD IDord-52333d0e1a2747388704d645e7e14910
Source noteuspto-grants-2004_01