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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
139165-52-9

N-[(1R,2R)-2-hydroxy-1,2-diphenylethyl]-Carbamic acid 1,1-dimethylethyl ester synthesis

3synthesis methods
2-Oxazolidinone, 4,5-diphenyl-, (4R,5R)-

23204-71-9
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N-[(1R,2R)-2-hydroxy-1,2-diphenylethyl]-Carbamic acid 1,1-dimethylethyl ester

139165-52-9
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-

Yield:-

Steps:

Multi-step reaction with 2 steps
1: NaH / tetrahydrofuran / 2 h / 25 °C
2: Cs2CO3 / aq. methanol

References:

Benedetti;Norbedo [Tetrahedron Letters,2000,vol. 41,# 51,p. 10071 - 10074]

24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
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N-[(1R,2R)-2-hydroxy-1,2-diphenylethyl]-Carbamic acid 1,1-dimethylethyl ester

139165-52-9
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References
N-[(1R,2S)-2-hydroxy-1,2-diphenylethyl]-Carbamic acid 1,1-dimethylethyl ester

142560-68-7
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N-[(1R,2R)-2-hydroxy-1,2-diphenylethyl]-Carbamic acid 1,1-dimethylethyl ester

139165-52-9
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References