تفاعل #1253191

ord-9ba2957f139848839a871eda7fd496db

معادلة التفاعل

C=CC(=O)OCCCCOC(=O)c1ccc(O)cc1
4-hydroxybenzoic acid 4-acryloyloxybutyl ester
C=CC(=O)OCCCCCCOc1ccc(-c2ccc(C(=O)O)cc2)cc1OC
4′-(6-acryloyloxyhexyloxy)-3′-methoxybiphenyl-4-carboxylic acid
ClCCCl
EDC
C=CC(=O)OCCCCCCOc1ccc(-c2ccc(C(=O)Oc3ccc(C(=O)OCCCCOC(=O)C=C)cc3)cc2)cc1OC
4′-(6-acryloyloxyhexyloxy)-3′-methoxybiphenyl-4-carboxylic acid 4-(4-acryloyloxybutoxycarbonyl)-phenyl ester

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىPurification of the residue by chromatography on silica gel
  2. 2
    أخرىcyclohexane/ethyl acetate (7:3) and recrystallisation once from ethanol

الإجراء التجريبي

The preparation is analogous to Example 1 from 2.64 g (10 mmol) of 4-hydroxybenzoic acid 4-acryloyloxybutyl ester, 3.99 g (10 mmol) of 4′-(6-acryloyloxyhexyloxy)-3′-methoxybiphenyl-4-carboxylic acid, 0.12 g (1 mmol) of DMAP and 2.11 g (11 mmol) of EDC. Purification of the residue by chromatography on silica gel using cyclohexane/ethyl acetate (7:3) and recrystallisation once from ethanol yields 4′-(6-acryloyloxyhexyloxy)-3′-methoxybiphenyl-4-carboxylic acid 4-(4-acryloyloxybutoxycarbonyl)-phenyl ester.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06613245B1uspto-grants-2003_09