(S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:(S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide
CAS No.:1092547-35-7
Molecular Formula:C₁₉H₂₃NO₃S
Molecular Weight:345.463
Hs Code.:

Synonyms:(S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

Suppliers and Price of (S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

Chemical Property:

Purity/Quality:

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Technology Process of (S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

There total 9 articles about (S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide 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:

Reference yield: 80.0%

: 82495-70-3
(2S)-2-p-toluenesulfonamido-3-phenylpropanol

: 106-95-6
allyl bromide

: 1092547-35-7
(S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

Guidance literature:: With potassium carbonate; In acetone; for 8 - 10h;
DOI:10.1016/j.tetasy.2008.09.007

Reference yield:

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 1092547-35-7
(S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / 6 h

2: potassium carbonate / N,N-dimethyl-formamide / 2 h / 0 °C

3: pyridine / 6 h / 0 - 20 °C

4: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 0 - 20 °C

With pyridine; lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/co200129t

Reference yield:

: 3182-95-4
L-Phenylalaninol

: 98-59-9
p-toluenesulfonyl chloride

: 1092547-35-7
(S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; triethylamine / dichloromethane / 0 - 20 °C

2: potassium carbonate / acetonitrile / 0.17 h / Reflux

With dmap; potassium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1002/anie.202109312