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3-hydroxymethyl-2,2,3-trimethyloxetane dihydrocinnamyl ester

Base Information
  • Chemical Name:3-hydroxymethyl-2,2,3-trimethyloxetane dihydrocinnamyl ester
  • CAS No.:845307-19-9
  • Molecular Formula:C16H22O3
  • Molecular Weight:262.349
  • Hs Code.:
3-hydroxymethyl-2,2,3-trimethyloxetane dihydrocinnamyl ester

Synonyms:3-hydroxymethyl-2,2,3-trimethyloxetane dihydrocinnamyl ester

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Chemical Property of 3-hydroxymethyl-2,2,3-trimethyloxetane dihydrocinnamyl ester
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Technology Process of 3-hydroxymethyl-2,2,3-trimethyloxetane dihydrocinnamyl ester

There total 4 articles about 3-hydroxymethyl-2,2,3-trimethyloxetane dihydrocinnamyl ester 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:
Multi-step reaction with 3 steps
1: 61 percent / potassium tert-butoxide; p-toluenesulfonyl chloride / tetrahydrofuran / 0.08 h / 20 °C
2: 55 percent / TBAF / tetrahydrofuran / 2 h / 20 °C
3: pyridine
With pyridine; potassium tert-butylate; tetrabutyl ammonium fluoride; p-toluenesulfonyl chloride; In tetrahydrofuran;
DOI:10.1021/ol047493n
Guidance literature:
Multi-step reaction with 4 steps
1: 42 percent / tetrahydrofuran / 0.17 h / 0 °C
2: 61 percent / potassium tert-butoxide; p-toluenesulfonyl chloride / tetrahydrofuran / 0.08 h / 20 °C
3: 55 percent / TBAF / tetrahydrofuran / 2 h / 20 °C
4: pyridine
With pyridine; potassium tert-butylate; tetrabutyl ammonium fluoride; p-toluenesulfonyl chloride; In tetrahydrofuran;
DOI:10.1021/ol047493n
Guidance literature:
Multi-step reaction with 2 steps
1: 55 percent / TBAF / tetrahydrofuran / 2 h / 20 °C
2: pyridine
With pyridine; tetrabutyl ammonium fluoride; In tetrahydrofuran;
DOI:10.1021/ol047493n
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