4-tert-Butylphenyl glycidyl ether, (-)-

Base Information

• Chemical Name: 4-tert-Butylphenyl glycidyl ether, (-)-
• CAS No.: 765305-18-8
• Molecular Formula: C₁₃H₁₈O₂
• Molecular Weight: 206.285
• UNII: 7TM4R6LSWW
• Nikkaji Number: J2.722.385K
• Wikidata: Q27268829

Synonyms:4-tert-Butylphenyl glycidyl ether, (-)-;765305-18-8;(2R)-2-[(4-tert-butylphenoxy)methyl]oxirane;7TM4R6LSWW;4-tert-Butylphenyl glycidyl ether, (R)-;(2R)-2-[[4-(1,1-Dimethylethyl)phenoxy]methyl]oxirane;Oxirane, ((4-(1,1-dimethylethyl)phenoxy)methyl)-, (2R)-;Oxirane, 2-((4-(1,1-dimethylethyl)phenoxy)methyl)-, (2R)-;UNII-7TM4R6LSWW;SCHEMBL2530840;HHRACYLRBOUBKM-LBPRGKRZSA-N;(-)-4-tert-butylphenyl glycidyl ether;(r)-2-(4-tert-butyl-phenoxymethyl)-oxirane;Q27268829

Chemical Property of 4-tert-Butylphenyl glycidyl ether, (-)-

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 206.130679813
• Heavy Atom Count: 15
• Complexity: 199

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C)(C)C1=CC=C(C=C1)OCC2CO2
• Isomeric SMILES: CC(C)(C)C1=CC=C(C=C1)OC[C@H]2CO2

Technology Process of 4-tert-Butylphenyl glycidyl ether, (-)-

There total 2 articles about 4-tert-Butylphenyl glycidyl 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:

Reference yield: 51.0%

(S)-epichlorohydrin (67843-74-7,24969-06-0,13403-37-7) + para-tert-butylphenol (98-54-4) → (R)-p-tert-butylphenyl glycidyl ether (765305-18-8)

Guidance literature:

With sodium hydroxide; In water; at 64 ℃; for 8h;

DOI:10.1016/j.bmc.2004.06.039

Reference yield:

→ (R)-p-tert-butylphenyl glycidyl ether (765305-18-8)

Guidance literature:

Reference yield: 99.0%

(R)-p-tert-butylphenyl glycidyl ether (765305-18-8) + methyl (2S,5R,6R)-6-(4-bromophenyl)-5-methylpiperidine-2-carboxylate (916915-02-1) → (3R,6R,7R,9aS)-6-(4-bromophenyl)-3-((4-tert-butylphenoxy)methyl)-7-methyl-hexahydropyrido[2,1-c][1,4]oxazin-1(6H)-one

Guidance literature:

With magnesium triflate; In acetonitrile; at 75 ℃;

DOI:10.1021/ol070321g

upstream raw materials:

(S)-epichlorohydrin

para-tert-butylphenol

Downstream raw materials:

(2R)-3-(p-tert-butylphenoxy)-1-(2-nitroimidazol-1-yl)-2-propanol

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