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4-Isoxazolecarboxylic acid, 4,5-dihydro-5-(hydroxymethyl)-3-(4-methoxyphenyl)-, ethyl ester, (4R,5R)-

Base Information
  • Chemical Name:4-Isoxazolecarboxylic acid, 4,5-dihydro-5-(hydroxymethyl)-3-(4-methoxyphenyl)-, ethyl ester, (4R,5R)-
  • CAS No.:216063-12-6
  • Molecular Formula:C14H17NO5
  • Molecular Weight:279.293
  • Hs Code.:
4-Isoxazolecarboxylic acid,
4,5-dihydro-5-(hydroxymethyl)-3-(4-methoxyphenyl)-, ethyl ester,
(4R,5R)-

Synonyms:

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Chemical Property of 4-Isoxazolecarboxylic acid, 4,5-dihydro-5-(hydroxymethyl)-3-(4-methoxyphenyl)-, ethyl ester, (4R,5R)-
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Technology Process of 4-Isoxazolecarboxylic acid, 4,5-dihydro-5-(hydroxymethyl)-3-(4-methoxyphenyl)-, ethyl ester, (4R,5R)-

There total 2 articles about 4-Isoxazolecarboxylic acid, 4,5-dihydro-5-(hydroxymethyl)-3-(4-methoxyphenyl)-, ethyl ester, (4R,5R)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With L-(+)-diisopropyl tartrate; diethylzinc; Yield given; Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 25 deg C, CHCl3, 1,4-dioxane;
DOI:10.1246/cl.1998.1023
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 25 ℃; for 1h; Yield given; Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1246/cl.1998.1023
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