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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | 5-Bromo-2-fluorobenzaldehyde | HCID 736327 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Bromo-2-fluorobenzylidene-2,2-dimethoxyethylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456169B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-ea9e706d576e4638bc718a6c87ecf8c6 |
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| Source note | uspto-grants-2008_11 |
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