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1-[6-allyl-4-(4-methoxy-benzyloxy)-3,5-dimethyl-tetrahydropyran-2-yl]-ethane-1,2-diol

Base Information Edit
  • Chemical Name:1-[6-allyl-4-(4-methoxy-benzyloxy)-3,5-dimethyl-tetrahydropyran-2-yl]-ethane-1,2-diol
  • CAS No.:201854-68-4
  • Molecular Formula:C20H30O5
  • Molecular Weight:350.455
  • Hs Code.:
  • Mol file:201854-68-4.mol
1-[6-allyl-4-(4-methoxy-benzyloxy)-3,5-dimethyl-tetrahydropyran-2-yl]-ethane-1,2-diol

Synonyms:1-[6-allyl-4-(4-methoxy-benzyloxy)-3,5-dimethyl-tetrahydropyran-2-yl]-ethane-1,2-diol

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Chemical Property of 1-[6-allyl-4-(4-methoxy-benzyloxy)-3,5-dimethyl-tetrahydropyran-2-yl]-ethane-1,2-diol Edit
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Technology Process of 1-[6-allyl-4-(4-methoxy-benzyloxy)-3,5-dimethyl-tetrahydropyran-2-yl]-ethane-1,2-diol

There total 26 articles about 1-[6-allyl-4-(4-methoxy-benzyloxy)-3,5-dimethyl-tetrahydropyran-2-yl]-ethane-1,2-diol 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:
Multi-step reaction with 14 steps
1.1: CF3SO3H / diethyl ether / 0.17 h / 0 °C
2.1: 371 mg / TBAF / tetrahydrofuran / 1 h / 20 °C
3.1: 91 percent / pyridine; DMAP / 3 h / 25 °C
4.1: OsO4; aq. NMO / acetone / 12 h / 20 °C
5.1: 3.2 g / aq. NaIO4 / tetrahydrofuran / 0 °C / pH 7
6.1: 94 percent / BF3*Et2O / CH2Cl2 / 2 h / -78 °C
7.1: 2,6-lutidine / CH2Cl2 / -50 °C
8.1: 347 mg / DIBALH / toluene; hexane / 2 h / -78 °C
9.1: DMSO; (COCl)2; Et3N / CH2Cl2 / 1.5 h / -70 - -30 °C
10.1: NaHMDS / tetrahydrofuran / 0.17 h / 0 °C
10.2: 309 mg / tetrahydrofuran / 1 h / -78 °C
11.1: 89 percent / DIBAL-H / toluene; hexane / 2 h / -78 °C
12.1: 98 percent / L-(+)-diethyl tartrate; Ti(i-OPr)4; t-BuOOH / 4 Angstroem molecular sieves / CH2Cl2; decane / 14.5 h / -25 - -20 °C
13.1: 86 percent / TBAF / tetrahydrofuran / 1.5 h / 0 °C
14.1: 76 percent / Ti(O-iPr)4 / benzene / 2 h / Heating
With pyridine; 2,6-dimethylpyridine; titanium(IV) isopropylate; tert.-butylhydroperoxide; dmap; sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; oxalyl dichloride; diethyl (2R,3R)-tartrate; trifluorormethanesulfonic acid; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; 4 A molecular sieve; In tetrahydrofuran; diethyl ether; decane; hexane; dichloromethane; acetone; toluene; benzene; 10.2: Wadsworth-Emmons olefination / 12.1: Sharpless reaction;
DOI:10.1039/b308305e
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