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19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether

Base Information
  • Chemical Name:19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether
  • CAS No.:337954-04-8
  • Molecular Formula:C55H104O9Si2
  • Molecular Weight:965.596
  • Hs Code.:
19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether

Synonyms:19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether

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Chemical Property of 19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether
Chemical Property:
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Technology Process of 19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether

There total 9 articles about 19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether 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:
Guidance literature:
(2S,3R,6S,1'S)-2-Decyl-3-tert-butyldimethylsilyloxy-6-(1'-tert-butyldimethylsilyloxy-3'-iodo)propyltetrahydropyran; With tert.-butyl lithium; In diethyl ether; at -105 ℃; for 0.0666667h;
With magnesium bromide; In tetrahydrofuran; at -100 - -40 ℃; for 2h;
(2S,5R)-2-Formyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)nonyl)tetrahydrofuran; In tetrahydrofuran; at -78 - -10 ℃; for 2h;
DOI:10.1002/1521-3773(20000616)39:12<2099::AID-ANIE2099>3.0.CO;2-Y
Guidance literature:
Multi-step reaction with 2 steps
1.1: 89 percent / (COCl)2; DMSO; NEt3 / CH2Cl2 / 1.75 h / -78 - -35 °C
2.1: tBuLi; magnesium bromide etherate / diethyl ether / 2 h / -105 - -40 °C
2.2: diethyl ether / 2 h / -78 - -10 °C
With oxalyl dichloride; tert.-butyl lithium; magnesium bromide ethyl etherate; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane; 1.1: Swern oxidation;
DOI:10.1002/1521-3765(20010302)7:5<993::AID-CHEM993>3.0.CO;2-S
Guidance literature:
Multi-step reaction with 4 steps
1.1: 97 percent / H2 / 5percent Pt/C / ethyl acetate / 6 h / 760.05 Torr
2.1: 95 percent / TBAF / tetrahydrofuran / 2.5 h
3.1: 89 percent / (COCl)2; DMSO; NEt3 / CH2Cl2 / 1.75 h / -78 - -35 °C
4.1: tBuLi; magnesium bromide etherate / diethyl ether / 2 h / -105 - -40 °C
4.2: diethyl ether / 2 h / -78 - -10 °C
With oxalyl dichloride; tetrabutyl ammonium fluoride; hydrogen; tert.-butyl lithium; magnesium bromide ethyl etherate; dimethyl sulfoxide; triethylamine; 5percent Pt/C; In tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate; 3.1: Swern oxidation;
DOI:10.1002/1521-3765(20010302)7:5<993::AID-CHEM993>3.0.CO;2-S
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