38132-31-9

Basic information

• Product Name: N-(2,6-diphenyltetrahydro-2H-4-pyranyl)-acetamide
• Synonyms: N-(2,6-diphenyltetrahydro-2H-4-pyranyl)-acetamide
• CAS NO: 38132-31-9
• Molecular Weight: 295.381
• Mol File: 38132-31-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: N-(2,6-diphenyltetrahydro-2H-4-pyranyl)-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,6-diphenyltetrahydro-2H-4-pyranyl)-acetamide(38132-31-9)
• EPA Substance Registry System: N-(2,6-diphenyltetrahydro-2H-4-pyranyl)-acetamide(38132-31-9)

Safety Data

• Hazardous Substances Data: 38132-31-9(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 74854-79-8 c-2,c-6-diphenyl-r-4-aminooxane 
• 80735-94-0 1-Phenyl-3-buten-1-ol 
• 100-52-7 benzaldehyde 
• 75-05-8 acetonitrile 
• 25830-15-3 trans-2,6-diphenyloxan-r-4-ol 
• 28144-10-7 r-2,cis-6-Diphenyl-4-oxanone Oxime 
• 762-72-1 allyl-trimethyl-silane 
• 18458-71-4 cis-2,6-diphenyltetrahydro-4H-pyran-4-one 
• 74854-86-7 trans-2,6-diphenyloxan-r-4-ol tosylate 

Relevant articles and documents

CeCl3·7H2O/AcCl-catalyzed Prins-Ritter reaction sequence: a novel synthesis of 4-amido tetrahydropyran derivatives

Homoallylic alcohols, carbonyl compounds and nitriles undergo a smooth tandem Prins-Ritter type cyclization in the presence of CeCl3·7H2O/AcCl at ambient temperature to produce 4-amido tetrahydropyrans in high yields with all cis-sel

Iodine/accl-catalyzed prins-ritter reaction: Synthesis of 4-amido tetrahydropyrans

Homoallylic alcohols, carbonyl compounds and nitriles undergo a smooth tandem Prins-Ritter type cyclization in the presence of iodine/AcCl at room temperature to produce 4-acetamido tetrahydropyrans in high yields with all cis-selectivity.

A Sakurai-Prins-Ritter reaction sequence for the diastereoselective synthesis of 4-amidotetrahydropyrans catalyzed by bismuth triflate

The synthesis of 4-amidotetrahydropyrans has been achieved by a single-step Sakurai-Prins-Ritter reaction sequence in a domino fashion by the reaction of an aldehyde and allyltrimethylsilane in acetonitrile using Bi(OTf)3 as catalyst. The prese