54750-12-8

Basic information

• Product Name: (2R,4S,5R)-2-chloro-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidin-2-one
• Synonyms: (2R,4S,5R)-2-chloro-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidin-2-one
• CAS NO: 54750-12-8
• Molecular Weight: 245.645
• Mol File: 54750-12-8.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: (2R,4S,5R)-2-chloro-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,4S,5R)-2-chloro-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidin-2-one(54750-12-8)
• EPA Substance Registry System: (2R,4S,5R)-2-chloro-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidin-2-one(54750-12-8)

Safety Data

• Hazardous Substances Data: 54750-12-8(Hazardous Substances Data)

Upstream product

• 90-82-4 pseudoephedrine 
• 321-98-2 (1S,2R)-(+)-ephedrine 
• 50-98-6 (-)-ephedrine hydrochloride 
• 299-42-3 ephedrine 
• 50-98-6 ephedrine hydrochloride 

Downstream Products

• 253433-65-7 (2S,2'S,4S,4'S,5R,5'R)-N,N'-bis(3,4-dimethyl-2-oxo-5-phenyl-2,3,2-oxazaphospholan-2-yl) (1R,2R)-cyclohexane-1,2-diamine 
• 54655-12-8 (2S,4S,5R)-3,4-Dimethyl-2,5-diphenyl-1,3,2-oxazaphospholidine 2-oxide 
• 123709-67-1 (2S,4S,5R)-3,4-dimethyl-2-hydrazido-5-phenyl-1,3,2-oxazaphospholidin-2-oxide 
• 184531-17-7 (3S,4R)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-[(1R,2R,6R)-1-((2S,4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yloxy)-7-oxa-bicyclo[4.1.0]hept-2-yl]-azetidin-2-one 
• 184531-18-8 (3R,4S)-3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-[(1S,2S,6S)-1-((2S,4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yloxy)-7-oxa-bicyclo[4.1.0]hept-2-yl]-azetidin-2-one 
• 184531-16-6 (3R,4S)-3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-[(S)-2-((2S,4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yloxy)-cyclohex-2-enyl]-azetidin-2-one 
• 184531-15-5 (3S,4R)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-[(R)-2-((2S,4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yloxy)-cyclohex-2-enyl]-azetidin-2-one 

Relevant articles and documents

Preparation of chiral phosphorus(V) reagents and their uses with borane in the enantioselective reduction of ketones

Chiral pentavalent phosphorus reagents 5-17 were prepared from POCl3 and ephedrine (or the related α-amino alcohols), followed by substitution with nucleophiles of phenylmagnesium bromide, alcohols, amines, diamines and triamines. The substitution reactions occurred in a stereospecific manner with retention of the configuration at the phosphorus center. The structures of these phosphorus(V) reagents were determined by spectral methods and verified by X-ray diffraction in several instances. These phosphorus(V) reagents were used with borane/dimethylsulfide complex in the enantioselective reduction of aromatic, aliphatic and heterocyclic ketones. The phosphorus(V) reagents likely functioned as Lewis bases to react with borane, forming in situ zwitterionic species as the chiral reducing agents. The reactions were generally carried out at 0 °C in tetrahydrofuran solution with a molar ratio of ketone/borane/phosphoramidate = 1:1:0.2 to afford secondary alcohols with modest enantioselectivity, up to 67% ee in the reduction of 4′-methylacetophenone.

Asymmetric Addition of Trimethylsilyl Cyanide to Benzaldehydes Catalyzed by Samarium(III) Chloride and Chiral Phosphorus(V) Reagents

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Highly stereocontrolled synthesis of enantiomeric 4-methoxy trinems via resolution of scalemic enol phosphates

Stereocontrolled syntheses of 4-methoxy trinem 2 and its enantiomer 3 were achieved using the ester enolate N-trimethylsilylimine approach. The key step was the resolution of racemic enolphosphates derived from ephedrine.