(S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide

Base Information

Chemical Name:(S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide
CAS No.:1350980-18-5
Molecular Formula:C₂₆H₂₄N₂O₆S
Molecular Weight:492.552
Hs Code.:

Synonyms:(S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide

Suppliers and Price of (S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide

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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-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide

Chemical Property:

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Technology Process of (S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide

There total 6 articles about (S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide 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: 24.0%

: 1350980-15-2
(S)-1-(1-amino-3-(benzyloxy)propan-2-yl)naphthalen-2-ol

: 1694-92-4
2-Nitrobenzenesulfonyl chloride

: 1350980-18-5
(S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide

Guidance literature:: With pyridine; at 40 - 60 ℃;
DOI:10.1016/j.tetlet.2011.10.105

Reference yield:

: 100-44-7
benzyl chloride

: 1350980-18-5
(S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium hydroxide

1.2: 10 - 60 °C

2.1: ammonium cerium (IV) nitrate; sodium nitrite / acetonitrile / 0 - 20 °C

3.1: C₂₈H₂₈F₆N₄S / toluene / 96 h / -50 °C / Molecular sieve

4.1: ammonium chloride; zinc / ethanol; water / 72 h / 20 °C

5.1: pyridine / 40 - 60 °C

With pyridine; ammonium cerium (IV) nitrate; C₂₈H₂₈F₆N₄S; ammonium chloride; potassium hydroxide; zinc; sodium nitrite; In ethanol; water; toluene; acetonitrile; 3.1: Friedel Crafts alkylation;
DOI:10.1016/j.tetlet.2011.10.105

Reference yield:

: 1350980-13-0
(S)-1-(1-(benzyloxy)-3-nitropropan-2-yl)naphthalen-2-ol

: 1350980-18-5
(S)-N-(3-(benzyloxy)-2-(2-hydroxynaphthalen-1-yl)propyl)-o-nitrobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium chloride; zinc / ethanol; water / 72 h / 20 °C

2: pyridine / 40 - 60 °C

With pyridine; ammonium chloride; zinc; In ethanol; water;
DOI:10.1016/j.tetlet.2011.10.105