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497863-61-3

N-[(3-Bromophenyl)methylene]-2,2-dimethoxyethanamine synthesis

1synthesis methods
3132-99-8 Synthesis
3-Bromobenzaldehyde

3132-99-8
514 suppliers
$5.00/10g

22483-09-6 Synthesis
Aminoacetaldehyde dimethyl acetal

22483-09-6
506 suppliers
$5.00/5g

-

Yield:-

Reaction Conditions:

in benzene; for 7 h;Reflux;

Steps:



A 1 L round bottom flask, outfitted with Dean-Stark adapter, a reflux condenser, and a PTFE-coated stirbar, was charged with 3-bromobenzaldehyde (50.0 g, 270 mmol, 1 equiv), aminoacetaldehyde dimethyl acetal (28.42 g, 1 equiv) and benzene (270 mL). The resulting solution became cloudy within 2 minutes and was heated at reflux until approximately 5 mL of water is collected in the Dean-Stark adapter (~7 hours). The solvent was then evaporated to afford the w-bromobenzalaminoacetal as a light yellow viscous liquid (~75 g) which was directly used in the subsequent cyclization step.

References:

WO2010/123545,2010,A2 Location in patent:Page/Page column 67-68

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