2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide

Base Information

Chemical Name:2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide
CAS No.:224313-64-8
Molecular Formula:C₁₄H₁₅NO₄S₂
Molecular Weight:325.409
Hs Code.:

Synonyms:2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide

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Chemical Property of 2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide

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Technology Process of 2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide

There total 6 articles about 2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide 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: 87.0%

: 224313-48-8
3-(methoxymethoxymethyl)-N-<(3-methoxyphenyl)methyl>-2-thiophenesulfonamide

: 224313-64-8
2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide

Guidance literature:: With toluene-4-sulfonic acid; In tetrahydrofuran; for 20h; Heating;
DOI:10.1002/jhet.5570360111

Reference yield: 85.0%

: 824-98-6
m-methoxybenzyl chloride

: 224313-67-1
2,3-dihydro-5H-thieno<2,3-e>-3,1,2-oxathiazepine 1,1-dioxide

: 224313-64-8
2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide

Guidance literature:: In dimethyl sulfoxide; for 20h; Ambient temperature;
DOI:10.1002/jhet.5570360111

Reference yield:

: 71637-34-8
3-hydroxymethyl-thiophene

: 224313-64-8
2,3-dihydro-2-<(3-methoxyphenyl)methyl>-5H-thieno<2,3-e>-4,1,2-oxathiazepine 1,1-dioxide

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) THF, reflux, 30 min, 2.) THF, reflux, 1 h

2: 1.) n-BuLi, 2.) SO₂, 3.) N-chlorosuccinimide

3: 66 percent / tetrahydrofuran / 0.08 h / 0 °C

4: 87 percent / p-TsOH / tetrahydrofuran / 20 h / Heating

With N-chloro-succinimide; n-butyllithium; sulfur dioxide; sodium hydride; toluene-4-sulfonic acid; In tetrahydrofuran;
DOI:10.1002/jhet.5570360111