C₂₅H₃₆N₂O₄S

Base Information

Chemical Name:C₂₅H₃₆N₂O₄S
CAS No.:1446528-61-5
Molecular Formula:C₂₅H₃₆N₂O₄S
Molecular Weight:460.638
Hs Code.:

C<sub>25</sub>H<sub>36</sub>N<sub>2</sub>O<sub>4</sub>S

Synonyms:C₂₅H₃₆N₂O₄S

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Chemical Property of C₂₅H₃₆N₂O₄S

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Technology Process of C₂₅H₃₆N₂O₄S

There total 5 articles about C₂₅H₃₆N₂O₄S 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: 98.0%

: 1446528-16-0
C₃₂H₄₀N₂O₅S

: 1446528-61-5
C₂₅H₃₆N₂O₄S

Guidance literature:: With water; sodium hydroxide; at 0 - 20 ℃; for 3h;
DOI:10.1002/adsc.201300135

Reference yield:

: 717-74-8
1,3,5-triisopropyl benzene

: 1446528-61-5
C₂₅H₃₆N₂O₄S

Guidance literature:: Multi-step reaction with 5 steps

1.1: chlorosulfonic acid / dichloromethane / 0.75 h / 0 - 20 °C

2.1: water; ammonia / dichloromethane / 12 h / 20 °C

3.1: neat (no solvent) / 16 h / 160 °C

4.1: C₂₈H₂₆F₆N₄O / diethyl ether / 96 h / -10 °C

4.2: 0.5 h / 20 °C

5.1: water; sodium hydroxide / 3 h / 0 - 20 °C

With chlorosulfonic acid; C₂₈H₂₆F₆N₄O; ammonia; water; sodium hydroxide; In diethyl ether; dichloromethane; 4.1: |Mannich Aminomethylation;
DOI:10.1002/adsc.201300135

Reference yield:

: 6553-96-4
2,4,6-triisopropylphenylsulfonyl chloride

: 1446528-61-5
C₂₅H₃₆N₂O₄S

Guidance literature:: Multi-step reaction with 4 steps

1.1: water; ammonia / dichloromethane / 12 h / 20 °C

2.1: neat (no solvent) / 16 h / 160 °C

3.1: C₂₈H₂₆F₆N₄O / diethyl ether / 96 h / -10 °C

3.2: 0.5 h / 20 °C

4.1: water; sodium hydroxide / 3 h / 0 - 20 °C

With C₂₈H₂₆F₆N₄O; ammonia; water; sodium hydroxide; In diethyl ether; dichloromethane; 3.1: |Mannich Aminomethylation;
DOI:10.1002/adsc.201300135