2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one

Base Information

• Chemical Name: 2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one
• CAS No.: 102520-18-3
• Molecular Formula: C₂₂H₂₈O₃
• Molecular Weight: 340.463
• Mol file: 102520-18-3.mol

Synonyms:2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one

Chemical Property of 2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one

There total 5 articles about 2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one 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%

2,4-di-tert-butyl-6-(1-phenylethenyl)phenol (102520-01-4) → 3,5-Di-tert-butyl-5-hydroxy-1-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-3-en-2-one (102520-12-7) + 2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one (102520-18-3)

Guidance literature:

With potassium tert-butylate; oxygen; In hexane; tert-butyl alcohol; for 5h; Ambient temperature;

DOI:10.1021/jo00362a018

Reference yield:

(3,5-di-tert-butyl-2-hydroxyphenyl)(phenyl)methanone (24242-58-8) → 2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one (102520-18-3)

Guidance literature:

Multi-step reaction with 3 steps

1: diethyl ether / 2.5 h / Heating

2: CH₃COOH / 0.17 h / Heating

3: 12 percent / t-BuOK, O₂ / 2-methyl-propan-2-ol; hexane / 5 h / Ambient temperature

With potassium tert-butylate; oxygen; acetic acid; In diethyl ether; hexane; tert-butyl alcohol;

DOI:10.1021/jo00362a018

Reference yield:

2,4-Di-tert-butyl-6-(1-hydroxy-1-phenyl-ethyl)-phenol → 2,6-Di-tert-butyl-2-hydroxy-4-(1-phenyl-vinyl)-7-oxa-bicyclo[4.1.0]hept-4-en-3-one (102520-18-3)

Guidance literature:

Multi-step reaction with 2 steps

1: CH₃COOH / 0.17 h / Heating

2: 12 percent / t-BuOK, O₂ / 2-methyl-propan-2-ol; hexane / 5 h / Ambient temperature

With potassium tert-butylate; oxygen; acetic acid; In hexane; tert-butyl alcohol;

DOI:10.1021/jo00362a018

upstream raw materials:

2,4-di-tert-butyl-6-(1-phenylethenyl)phenol

(3,5-di-tert-butyl-2-hydroxyphenyl)(phenyl)methanone

2,4-Di-tert-butyl-6-(2-methyl-1-phenyl-propenyl)-phenol