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51632-06-5

5-HYDROXYMETHYLINDANE synthesis

10synthesis methods
30084-91-4 Synthesis
INDAN-5-CARBOXALDEHYDE

30084-91-4
107 suppliers
$74.00/250mg

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Yield:51632-06-5 96%

Reaction Conditions:

Stage #1: indan-5-carbaldehydewith sodium tetrahydroborate in ethanol at 0; for 0.5 h;
Stage #2: with hydrogenchloride in water; pH=2;

Steps:

10.2

To a stirred solution of Indan-5-carbaldehyde (2 g, 13.69 mmol) in EtOH (20 ml) at 0 0C was added sodium borohydride (676 mg, 17.80 mmol). The reaction was continued for 30 min. and monitored by thin layer chromatography. The reaction mixture was concentrated, acidified by addition of 2N HCl to pH 2. It was extracted with dichloromethane (2x 25 ml). The combined organic layer was washed with brine (25 ml), dried over anhydrous sodium sulfate and concentrated under vacuo to afford colorless oil (1.95 g , 96 %).

References:

WO2009/109999,2009,A1 Location in patent:Page/Page column 60

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