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850222-41-2

850222-41-2 synthesis

3synthesis methods
2743-38-6 Synthesis
Dibenzoyl-L-tartaric acid

2743-38-6
530 suppliers
$10.00/5g

(R)-3-(dimethylamino)-1-(3-methoxyphenyl)-2-methylpropan-1-one

1217854-15-3
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850222-41-2

850222-41-2
11 suppliers
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Yield:850222-41-2 80.5%

Reaction Conditions:

in acetone at 35 - 40; for 27 h;Purification / work up;Resolution of racemate;

Steps:

a''.1.a

1. a. Preparation of (S)-3-(dimethylamino)-1-(3-methoxyphenyl)-2- methylpropan-1-one (2R,3R)-O,O'-dibenzoyltartrate in acetone; (2R,3R)-O,O'-Dibenzoyl tartaric acid monohydrate (189.1 g, 0.5 mol) was dissolved in acetone (550 mL) in a 2 L reaction plant equipped with a mechanical stirrer, temperature measuring equipment and an oil bath and 3-(dimethylamino)-1-(3- methoxyphenyl)-2-methylpropan-1-one (110.6 g, 0.5 mol) was added. The reaction mixture was heated to 35 0C to 40 0C for 27 hours and allowed to cool to 25 0C. The suspension was siphoned off and (S)-3-(dimethylamino)-1-(3-methoxyphenyl)-2- methylpropan-1-one (2R,3R)-O,O'-dibenzoyltartrate was obtained as a colorless solid (233.2 g, 80.5 %, ee 96.9 %, ee = enantiomeric excess).

References:

WO2008/12047,2008,A1 Location in patent:Page/Page column 19