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tert-butyl (2S,4R,6S)-2-(4-methoxyphenyl)-6-(2-oxoethyl)-[1,3]dioxan-4-ylacetate

Base Information
  • Chemical Name:tert-butyl (2S,4R,6S)-2-(4-methoxyphenyl)-6-(2-oxoethyl)-[1,3]dioxan-4-ylacetate
  • CAS No.:625124-68-7
  • Molecular Formula:C19H26O6
  • Molecular Weight:350.412
  • Hs Code.:
tert-butyl (2S,4R,6S)-2-(4-methoxyphenyl)-6-(2-oxoethyl)-[1,3]dioxan-4-ylacetate

Synonyms:tert-butyl (2S,4R,6S)-2-(4-methoxyphenyl)-6-(2-oxoethyl)-[1,3]dioxan-4-ylacetate

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Chemical Property of tert-butyl (2S,4R,6S)-2-(4-methoxyphenyl)-6-(2-oxoethyl)-[1,3]dioxan-4-ylacetate
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Technology Process of tert-butyl (2S,4R,6S)-2-(4-methoxyphenyl)-6-(2-oxoethyl)-[1,3]dioxan-4-ylacetate

There total 8 articles about tert-butyl (2S,4R,6S)-2-(4-methoxyphenyl)-6-(2-oxoethyl)-[1,3]dioxan-4-ylacetate 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:
tert-butyl (3R,5S)-[6-allyl-2-(4-methoxyphenyl)-[1,3]dioxan-4-yl]acetate; With ozone; In methanol; dichloromethane; for 1h;
With tributylphosphine; In methanol; dichloromethane; for 0.166667h;
DOI:10.1021/ja030316h
Guidance literature:
Multi-step reaction with 8 steps
1.1: LDA / tetrahydrofuran; hexane / 1 h
1.2: tetrahydrofuran; hexane / 0.5 h / Heating
2.1: 87.3 g / Et2BOMe; NaBH4 / tetrahydrofuran; methanol
3.1: PPTS / CH2Cl2 / 2.5 h / Heating
4.1: 33.0 g / tetrabutylammonium fluoride trihydrate / tetrahydrofuran / 1 h
5.1: Et3N / CH2Cl2 / 4.25 h / 20 °C
6.1: NaI; NaHCO3; Na2SO3 / butan-2-one / 16 h / Heating
7.1: Li2CuCl4 / tetrahydrofuran
8.1: O3 / CH2Cl2; methanol / 1 h
8.2: 33.6 g / tributylphosphine / CH2Cl2; methanol / 0.17 h
With sodium tetrahydroborate; dilithium tetrachlorocuprate; diethyl methoxy borane; tetrabutyl ammonium fluoride; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; ozone; triethylamine; sodium iodide; sodium sulfite; lithium diisopropyl amide; In tetrahydrofuran; methanol; hexane; dichloromethane; butanone; 1.2: Claisen condensation;
DOI:10.1021/ja030316h
Guidance literature:
Multi-step reaction with 4 steps
1.1: Et3N / CH2Cl2 / 4.25 h / 20 °C
2.1: NaI; NaHCO3; Na2SO3 / butan-2-one / 16 h / Heating
3.1: Li2CuCl4 / tetrahydrofuran
4.1: O3 / CH2Cl2; methanol / 1 h
4.2: 33.6 g / tributylphosphine / CH2Cl2; methanol / 0.17 h
With dilithium tetrachlorocuprate; sodium hydrogencarbonate; ozone; triethylamine; sodium iodide; sodium sulfite; In tetrahydrofuran; methanol; dichloromethane; butanone;
DOI:10.1021/ja030316h
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