N-t-butyl-6-[1-(4-methoxyphenyl)-1-hydroxymethyl]-benzo[d][1,3]dioxole-5-sulfonamide

Base Information

Chemical Name:N-t-butyl-6-[1-(4-methoxyphenyl)-1-hydroxymethyl]-benzo[d][1,3]dioxole-5-sulfonamide
CAS No.:1222561-38-7
Molecular Formula:C₁₉H₂₃NO₆S
Molecular Weight:393.461
Hs Code.:

Synonyms:N-t-butyl-6-[1-(4-methoxyphenyl)-1-hydroxymethyl]-benzo[d][1,3]dioxole-5-sulfonamide

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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 N-t-butyl-6-[1-(4-methoxyphenyl)-1-hydroxymethyl]-benzo[d][1,3]dioxole-5-sulfonamide

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Technology Process of N-t-butyl-6-[1-(4-methoxyphenyl)-1-hydroxymethyl]-benzo[d][1,3]dioxole-5-sulfonamide

There total 1 articles about N-t-butyl-6-[1-(4-methoxyphenyl)-1-hydroxymethyl]-benzo[d][1,3]dioxole-5-sulfonamide 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: 88.0%

: 1222561-32-1
C₁₁H₁₅NO₄S

: 123-11-5
4-methoxy-benzaldehyde

: 1222561-38-7
N-t-butyl-6-[1-(4-methoxyphenyl)-1-hydroxymethyl]-benzo[d][1,3]dioxole-5-sulfonamide

Guidance literature:: C₁₁H₁₅NO₄S; With n-butyllithium; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h; Inert atmosphere;

4-methoxy-benzaldehyde; In tetrahydrofuran; hexane; for 1h; Inert atmosphere;

With water; ammonium chloride; In tetrahydrofuran; hexane;
DOI:10.3987/COM-09-11884

Reference yield: 91.0%

: 1222561-38-7
N-t-butyl-6-[1-(4-methoxyphenyl)-1-hydroxymethyl]-benzo[d][1,3]dioxole-5-sulfonamide

: 1222561-45-6
3-(4-methoxyphenyl)-2,3-dihydro[1,3]dioxolo[4,5-f][1,2]benzisothiazole 1,1-dioxide

Guidance literature:: With chloro-trimethyl-silane; iodine; sodium iodide; In acetonitrile; at 20 ℃; Inert atmosphere; Reflux;
DOI:10.3987/COM-09-11884