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(R)-N-allyl-N-phenyl tert-butanesulfinamide

Base Information
  • Chemical Name:(R)-N-allyl-N-phenyl tert-butanesulfinamide
  • CAS No.:1372133-79-3
  • Molecular Formula:C13H19NOS
  • Molecular Weight:237.366
  • Hs Code.:
(R)-N-allyl-N-phenyl tert-butanesulfinamide

Synonyms:(R)-N-allyl-N-phenyl tert-butanesulfinamide

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Chemical Property of (R)-N-allyl-N-phenyl tert-butanesulfinamide
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Technology Process of (R)-N-allyl-N-phenyl tert-butanesulfinamide

There total 4 articles about (R)-N-allyl-N-phenyl tert-butanesulfinamide 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 sodium hydride; In N,N-dimethyl-formamide; at 25 ℃; for 0.25h; Schlenk technique;
DOI:10.1021/acs.orglett.1c03221
Guidance literature:
Multi-step reaction with 2 steps
1.1: tris-(dibenzylideneacetone)dipalladium(0); di-tert-butyl (2',4',6'-triisopropylbiphenyl-2-yl)phosphine; water; sodium hydroxide / toluene / 20 h / 90 °C / Inert atmosphere
2.1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / Cooling with ice; Inert atmosphere
2.2: Inert atmosphere
With tris-(dibenzylideneacetone)dipalladium(0); di-tert-butyl (2',4',6'-triisopropylbiphenyl-2-yl)phosphine; water; sodium hydride; sodium hydroxide; In tetrahydrofuran; toluene; mineral oil;
DOI:10.1021/jo3003584
Guidance literature:
Multi-step reaction with 2 steps
1: dihydroquinine / chloroform; 1,2-dichloro-ethane / 180 h / -40 °C / Schlenk technique; Molecular sieve; Resolution of racemate
2: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 25 °C / Schlenk technique
With sodium hydride; dihydroquinine; In chloroform; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1021/acs.orglett.1c03221
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