反应 #2006425

ord-d9df4f0fa1fd4a7386345a283e893c47

反应方程式

O=C(CCc1ccc(C=CCc2ccccc2)cc1)NO
N-hydroxy-3-[4-(3-phenyl-1-propenyl)-phenyl]-propanamide
O=C(CCc1ccc(CC=Cc2ccccc2)cc1)NO
N-hydroxy-3-[4-(3-phenyl-2-propenyl)-phenyl]-propanamide
O=C(O)c1ccc(C=CCc2ccccc2)cc1.O=C(O)c1ccc(CC=Cc2ccccc2)cc1
olefins
O=C(O)c1ccc(C=CCc2ccccc2)cc1.O=C(O)c1ccc(CC=Cc2ccccc2)cc1
4(3-Phenylpropenyl)-benzoic Acid 4-(3-Phenyl-2-propenyl)-benzoic Acid
O=C(CCc1ccc(CCCc2ccccc2)cc1)NO
title compound
收率 99.0%
O=C(CCc1ccc(CCCc2ccccc2)cc1)NO
N-Hydroxy-3[4-(3-phenylpropyl)-phenyl]-propanamide
收率 99.0%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Following a procedure analogous to that described in Example 24, step 2, but substituting the mixture of N-hydroxy-3-[4-(3-phenyl-1-propenyl)-phenyl]-propanamide and N-hydroxy-3-[4-(3-phenyl-2-propenyl)-phenyl]-propanamide (155 mg, 0.55 mmol) for olefins 54, 155.4 mg (99%) of the title compound was obtained.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE043343E1uspto-grants-2012_05