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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272777Generated: October 31, 2026

Aminoacetaldehyde dimethyl acetal → 5-Bromo-2-fluorobenzylidene-2,2-dimethoxyethylamine

https://huagongshe.com/reaction/272777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactant5-Bromo-2-fluorobenzaldehydeHCID 736327—
SolventTolueneHCID 1140—
Product5-Bromo-2-fluorobenzylidene-2,2-dimethoxyethylamineHCID 69215896—

Reaction Steps

A mixture of 5-bromo-2-fluorobenzaldehyde (15 g, 74 mmol) and 2,2-dimethoxy-ethylamine (7.77 g, 74 mmol) in toluene (142 mL) was heated to reflux for 30 minutes using a Dean-Stark trap to remove water. The solution was then concentrated under vacuum to provide 5-bromo-2-fluorobenzylidene-2,2-dimethoxyethylamine. 5-Bromo-2-fluorobenzylidene-2,2-dimethoxyethylamine and cold concentrated sulfuric acid (28 mL) were added separately, dropwise, over a period of 20 minutes to concentrated sulfuric acid (83 mL) at 140° C. The mixture was stirred at 135° C. for 30 minutes, allowed to cool, and carefully poured onto ice. Filtered to remove solids and the mixture was washed with dichloromethane. The aqueous layer was made basic by cautious addition of 50% sodium hydroxide solution, and extracted with diethyl ether. Combined ether layers were dried (MgSO4), filtered and concentrated under vacuum to provide 310 mg (2%) of the desired product. MS (ESI) m/e 226 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456169B2
Source datasetuspto-grants-2008_11
ORD IDord-ea9e706d576e4638bc718a6c87ecf8c6
Source noteuspto-grants-2008_11