1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol

Base Information

• Chemical Name: 1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol
• CAS No.: 256469-30-4
• Molecular Formula: C₂₀H₃₈O₂Si
• Molecular Weight: 338.606
• Mol file: 256469-30-4.mol

Synonyms:1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol

Chemical Property of 1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol

There total 7 articles about 1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol 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: 90.0%

1-bromo-4-butene (5162-44-7) + 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enone (256469-27-9) → 1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol (256469-30-4)

Guidance literature:

With cerium(III) chloride; magnesium; In tetrahydrofuran; at 0 - 20 ℃; for 15h;

DOI:10.1002/(SICI)1099-0690(199912)1999:12<3241::AID-EJOC3241>3.0.CO;2-9

Reference yield:

ethylene glycole monoacetal of 2,2-dimethylcyclohexane-1,3-dione (14782-52-6) → 1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol (256469-30-4)

Guidance literature:

Multi-step reaction with 6 steps

1: 85 percent / LiHMDS / tetrahydrofuran / 3 h / 0 °C

2: 95 percent / LiCl; DBU / Pd(PPh₃)4 / tetrahydrofuran / 20 °C / Heating

3: 100 percent / 9-BBN; H₂O₂; NaOH / tetrahydrofuran; ethanol / 3 h / Heating

4: 99 percent / TsOH / tetrahydrofuran; H₂O / 18 h / Heating

5: 99 percent / Et₃N; DMAP / CH₂Cl₂ / 15 h / 20 °C

6: 90 percent / Mg; CeCl₃ / tetrahydrofuran / 15 h / 0 - 20 °C

With dmap; sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; cerium(III) chloride; dihydrogen peroxide; toluene-4-sulfonic acid; magnesium; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; lithium chloride; lithium hexamethyldisilazane; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; ethanol; dichloromethane; water; 1: Substitution / 2: Substitution / 3: hydroboration / 4: Elimination / 5: silylation / 6: Grignard reaction;

DOI:10.1002/(SICI)1099-0690(199912)1999:12<3241::AID-EJOC3241>3.0.CO;2-9

Reference yield:

6,6-dimethyl-1,4-dioxaspiro[4.5]dec-7-en-7-yl trifluoromethanesulfonate (256469-23-5) → 1-but-3-enyl-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enol (256469-30-4)

Guidance literature:

Multi-step reaction with 5 steps

1: 95 percent / LiCl; DBU / Pd(PPh₃)4 / tetrahydrofuran / 20 °C / Heating

2: 100 percent / 9-BBN; H₂O₂; NaOH / tetrahydrofuran; ethanol / 3 h / Heating

3: 99 percent / TsOH / tetrahydrofuran; H₂O / 18 h / Heating

4: 99 percent / Et₃N; DMAP / CH₂Cl₂ / 15 h / 20 °C

5: 90 percent / Mg; CeCl₃ / tetrahydrofuran / 15 h / 0 - 20 °C

With dmap; sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; cerium(III) chloride; dihydrogen peroxide; toluene-4-sulfonic acid; magnesium; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; ethanol; dichloromethane; water; 1: Substitution / 2: hydroboration / 3: Elimination / 4: silylation / 5: Grignard reaction;

DOI:10.1002/(SICI)1099-0690(199912)1999:12<3241::AID-EJOC3241>3.0.CO;2-9

upstream raw materials:

1-bromo-4-butene

3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-cyclohex-3-enone

ethylene glycole monoacetal of 2,2-dimethylcyclohexane-1,3-dione

3-(2-hydroxyethyl)-2,2-dimethylcyclohex-3-en-1-one

Downstream raw materials:

1-but-3-enyl-3-(2-iodo-ethyl)-2,2-dimethyl-cyclohex-3-enol

(5-but-3-enyl-5-hydroxy-6,6-dimethyl-cyclohex-1-enyl)-acetaldehyde oxime

1-allyl-2,2-dimethyl-3-(2-nitro-ethyl)-cyclohex-3-enol

1-allyl-3-(2-iodo-ethyl)-2,2-dimethyl-cyclohex-3-enol