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dibenzyl (1R,2S)-2-(p-toluenesulfonyloxymethyl)cyclopropylphosphonate

Base Information
  • Chemical Name:dibenzyl (1R,2S)-2-(p-toluenesulfonyloxymethyl)cyclopropylphosphonate
  • CAS No.:887232-71-5
  • Molecular Formula:C25H27O6PS
  • Molecular Weight:486.526
  • Hs Code.:
dibenzyl (1R,2S)-2-(p-toluenesulfonyloxymethyl)cyclopropylphosphonate

Synonyms:dibenzyl (1R,2S)-2-(p-toluenesulfonyloxymethyl)cyclopropylphosphonate

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Chemical Property of dibenzyl (1R,2S)-2-(p-toluenesulfonyloxymethyl)cyclopropylphosphonate
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Technology Process of dibenzyl (1R,2S)-2-(p-toluenesulfonyloxymethyl)cyclopropylphosphonate

There total 4 articles about dibenzyl (1R,2S)-2-(p-toluenesulfonyloxymethyl)cyclopropylphosphonate 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 trimethylamine hydrochloride; triethylamine; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1021/jm051177c
Guidance literature:
Multi-step reaction with 2 steps
1.1: n-BuLi / hexane; tetrahydrofuran / 0.25 h / -78 °C
1.2: 39 percent / BF3*OEt2 / hexane; tetrahydrofuran / 0.25 h / -78 °C
2.1: 85 percent / Et3N; Me3N*HCl / CH2Cl2 / 1 h / 0 °C
With n-butyllithium; trimethylamine hydrochloride; triethylamine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/jm051177c
Guidance literature:
Multi-step reaction with 3 steps
1.1: 81 percent / t-BuOK / tetrahydrofuran / 3 h / 0 °C
2.1: n-BuLi / hexane; tetrahydrofuran / 0.25 h / -78 °C
2.2: 39 percent / BF3*OEt2 / hexane; tetrahydrofuran / 0.25 h / -78 °C
3.1: 85 percent / Et3N; Me3N*HCl / CH2Cl2 / 1 h / 0 °C
With n-butyllithium; potassium tert-butylate; trimethylamine hydrochloride; triethylamine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/jm051177c
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