(6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol

Base Information

Chemical Name:(6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol
CAS No.:1361253-08-8
Molecular Formula:C₂₂H₂₉NO₄SSi
Molecular Weight:431.628
Hs Code.:

Synonyms:(6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol

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Chemical Property of (6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol

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Technology Process of (6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol

There total 4 articles about (6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol 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: 65.0%

: 2942-13-4
6-methoxy-1,3-benzothiazole

: 69404-94-0
O-tert-butyldimethylsilylvanillin

: 1361253-08-8
(6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol

Guidance literature:: 6-methoxy-1,3-benzothiazole; With n-butyllithium; In tetrahydrofuran; hexane; for 1h; Cooling with acetone-dry ice;

O-tert-butyldimethylsilylvanillin; In tetrahydrofuran; hexane; for 2h; Cooling with acetone-dry ice;
DOI:10.1021/jm201711b

Reference yield: 65.0%

: 1361253-08-8
(6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol

Guidance literature:

Reference yield:

: 121-33-5,8014-42-4
vanillin

: 1361253-08-8
(6-methoxy-1,3-benzothiazol-2-yl)[3-methoxy-4-(tert-butyldimethylsilanyloxy)phenyl]methanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1H-imidazole / N,N-dimethyl-formamide / 20 h / 20 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / Cooling with acetone-dry ice

2.2: 2 h / Cooling with acetone-dry ice

With 1H-imidazole; n-butyllithium; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1021/jm201711b