Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575039Generated: October 29, 2026

Aminoacetaldehyde dimethyl acetal → HCID 178495872, compound

https://huagongshe.com/reaction/575039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantHCID 86693069HCID 86693069—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
ProductHCID 178495872HCID 178495872107.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a 100-mL 3-necked round-bottom flask was placed a solution of 5-bromo-8-chloro-4-fluoro-9-azatricyclo[8.1.1.0[2,7]]dodeca-2,4,6,8-tetraene (3.75 g, 13.00 mmol, 1.00 equiv) in n-BuOH (50 mL) and 2,2-dimethoxyethan-1-amine (1.5 g, 14.27 mmol, 1.10 equiv). The resulting solution was stirred at 100° C. for 1.5, diluted with 50 mL of water and extracted with 1×50 mL of ethyl acetate. The organic layers were combined and concentrated under vacuum to afford 5.0 g (crude) of 5-bromo-N-(2,2-dimethoxyethyl)-4-fluoro-9-azatricyclo[8.1.1.0[2,7]]dodeca-2,4,6,8-tetraen-8-amine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-1340da24d82244e1a381053ad78141d0
Source noteuspto-grants-2015_05