반응 #828727

ord-3336992df8f542dc842e8ce196bb669e

반응 방정식

CCOC(=O)C(Cc1ccccc1)C(=O)OCC
diethyl benzylmalonate
[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminum hydride
OCC(CO)Cc1ccccc1
2-benzyl-1,3-propanediol

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

Accordingly, diethyl benzylmalonate (1) is reduced with lithium aluminum hydride to afford 2-benzyl-1,3-propanediol (2) which is treated with an equimolar amount of tert-butyldimethylsilyl chloride to give the monoprotected alcohol 3. Swern (dimethylsulfoxide/oxalyl chloride) oxidation of 3 provides the aldehyde 4 which is condensed with the Wittig reagent methyl (triphenylphosphonylidene) acetate to give 6. Conversion of the alcohol 6 to the mesylate 7 followed by azide displacement affords 8 which is sequentially reduced and Boc protected to give 9. Jones oxidation of the tert-butyldimethylsilyl ether 9 provides the Boc protected substituted ω-aminoalkenoic acid 10.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05552383uspto-grants-1996_09