Dimethyl malonate → HCID 10081946, compound

HRID 916295Notes

Reaction equation

HRID 916295 reaction equation
[C:1]1(=[O:6])[CH2:5][CH2:4][CH:3]=[CH:2]1.[C:7]([O:14][CH3:15])(=[O:13])[CH2:8][C:9]([O:11][CH3:12])=[O:10]>CC(C)=O>[CH3:12][O:11][C:9]([CH:8]([C:7]([O:14][CH3:15])=[O:13])[C@H:3]1[CH2:4][CH2:5][C:1](=[O:6])[CH2:2]1)=[O:10]

Participants

4

Reactant 2

HCID 7943Dimethyl malonateHCID 135882-Cyclopenten-1-one

Product 1

HCID 10081946HCID 10081946, compoundYield 99.4%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Conditions

Temperature
40 °C

Procedure

Under an atmosphere of argon, 12.0 mg (0.02 mmol, S/C=50) of RuH[(R,R)-Tsdpen] (1,3,5-trimethylbenzene), 84 μL (1.0 mmol) of 2-cyclopentenone, 114 μL (1.0 mmol) of dimethyl malonate, and 1 mL of acetone were placed in a 20 mL Schlenk tube and stirred at 40° C. for 24 hours. This solution was purified by flash column chromatography (hexane/acetone=90/10, SiO2) to give 213 mg (99% yield) of the title compound. The optical purity was measured by HPLC (CHIRALPAK AS manufactured by Daicel Chemical Industries, Ltd., hexane:2-propanol=80:20, flow rate 1.0 mL/min, detection at 210 nm) and it was found to be 89% ee.

Workup

  1. customThis solution was purified by flash column chromatography (hexane/acetone=90/10, SiO2)

Sources & evidence

ORD record
ord-06aead46a2af49f1828c46619585febd
Source dataset
uspto-grants-2007_09
Patent number
US07268250B2

Reaction notes

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