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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741071Generated: October 30, 2026

Triethylamine → HCID 21833710, compound

https://huagongshe.com/reaction/1741071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-1-propeneHCID 11203—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Bromo-3-methylbenzaldehyde oximeHCID 73847954—
SolventDimethylformamideHCID 6228—
ProductHCID 21833710HCID 2183371027.3%

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of 4-bromo-3-methylbenzaldehyde oxime (D81) (2.68 g, 0.0125 mol) in dry dimethylformamide (30 ml) was treated over 15 minutes with N-bromosuccinimide (636 mg, 0.00357 mol), and reaction mixture stirred for 2.5 hours, then cooled to -15° C. 2-Chloropropene (3.45 ml, 0.0405 mol) was added in a single portion, followed by dropwise addition of triethylamine (1.35 ml, 0.0097 mol) in dry dimethylformamide (10 ml) over 0.5 hours maintaining the temp. at -10° C. The mixture was stirred at 0° C. for 1 hour, then stirred at room temperature overnight. The solvent was evaporated under reduced pressure and the residue partitioned between K2CO3 solution and chloroform. The organic phase was dried (Na2SO4) and evaporated under reduced pressure and the residue purified by chromatography on silica gel eluting with 60-80 petroleum-ether and ethyl acetate, to afford the title compound (246 mg, 8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972951
Source datasetuspto-grants-1999_10
ORD IDord-b61a16707a66440c9dfafb8938cc2f0e
Source noteuspto-grants-1999_10