thiomorpholin-4-yl benzoate

Base Information

Chemical Name:thiomorpholin-4-yl benzoate
CAS No.:1446513-60-5
Molecular Formula:C₁₁H₁₃NO₂S
Molecular Weight:223.296
Hs Code.:

Synonyms:thiomorpholin-4-yl benzoate

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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 thiomorpholin-4-yl benzoate

Chemical Property:

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Technology Process of thiomorpholin-4-yl benzoate

There total 1 articles about thiomorpholin-4-yl benzoate 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:

: 98-88-4
benzoyl chloride

: 1446513-60-5
thiomorpholin-4-yl benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: dihydrogen peroxide / Inert atmosphere

2: potassium carbonate / dichloromethane / 20 °C / Inert atmosphere

With dihydrogen peroxide; potassium carbonate; In dichloromethane;
DOI:10.1039/c9cc09265j

Reference yield: 85.0%

: 14933-97-2
N-phenylbenzenesulfinamide

: 1446513-60-5
thiomorpholin-4-yl benzoate

: 4-(N-phenylphenylsulfonimidoyl)thiomorpholine

Guidance literature:: With copper(I) bromide; In acetonitrile; at 80 ℃; for 12h; Inert atmosphere; Sealed tube;
DOI:10.1002/anie.201810548

Reference yield: 85.0%

: 22825-21-4
3,3-diphenylcyclopropene

: 1446513-60-5
thiomorpholin-4-yl benzoate

: 202864-71-9
5,5-dimethyl-2-(β-phenylethenyl)-1,3,2-dioxaborinane

: 4-((1R,3R)-2,2-diphenyl-3-((E)-styryl)cyclopropyl)thiomorpholine

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; copper(l) chloride; sodium t-butanolate; (R,R)-1,2-bis(2,5-diphenylphospholanyl)ethane; In tetrahydrofuran; at 20 ℃; enantioselective reaction; Glovebox; Inert atmosphere;
DOI:10.1039/d0cc01060j