N-benzyl N-allyl amino-2 ethanethiol-1

Base Information

• Chemical Name: N-benzyl N-allyl amino-2 ethanethiol-1
• CAS No.: 81829-66-5
• Molecular Formula: C₁₂H₁₇NS
• Molecular Weight: 207.34
• Mol file: 81829-66-5.mol

Synonyms:

Chemical Property of N-benzyl N-allyl amino-2 ethanethiol-1

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-benzyl N-allyl amino-2 ethanethiol-1

There total 2 articles about N-benzyl N-allyl amino-2 ethanethiol-1 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: 60.0%

thirane (420-12-2) + Allylbenzylamine (4383-22-6) → N-benzyl N-allyl amino-2 ethanethiol-1 (81829-66-5)

Guidance literature:

In benzene;

Reference yield:

benzyl bromide (100-39-0) → N-benzyl N-allyl amino-2 ethanethiol-1 (81829-66-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 78 percent / 48 h / Heating

2: 60 percent / benzene

In benzene;

Reference yield:

N-benzyl N-allyl amino-2 ethanethiol-1 (81829-66-5) → 3-Benzyl-2-ethyl-thiazolidine (81829-71-2) + 4-Benzyl-2-methyl-thiomorpholine (81829-72-3)

Guidance literature:

In cyclohexane; at 80 ℃; for 36h; Yield given. Yields of byproduct given; Irradiation;

upstream raw materials:

thirane

Allylbenzylamine

benzyl bromide

Downstream raw materials:

4-benzyl-[1,4]thiazepane

3-Benzyl-2-ethyl-thiazolidine

4-Benzyl-2-methyl-thiomorpholine

Refernces