(E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-one

Base Information

Chemical Name:(E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-one
CAS No.:121468-86-8
Molecular Formula:C₁₉H₃₄O₂Si
Molecular Weight:322.563
Hs Code.:

Synonyms:(E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-one

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Chemical Property of (E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-one

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Technology Process of (E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-one

There total 10 articles about (E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-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: 98.0%

: 121401-86-3,121429-39-8
(E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-ol

: 121468-86-8
(E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-one

Guidance literature:: With manganese(IV) oxide; In dichloromethane; under dim red light;
DOI:10.1016/S0040-4039(00)86036-0

Reference yield:

: 116-26-7
safranal

: 121468-86-8
(E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-one

Guidance literature:: Multi-step reaction with 10 steps

1: 92 percent / sodium borohydride / ethanol

2: 98 percent / H⁽¹⁺⁾

3: 1.) (-)-diisopinocamphenyl borane, 2.) H₂O₂/NaOH

4: H⁽¹⁺⁾ / acetone

5: 50 percent / PDC / CH₂Cl₂; dioxane / under dim red light

6: 78 percent / NaH / under dim red light

7: 95 percent / imidazole / dimethylformamide / under dim red light

8: 70 percent / DIBAL / under dim red light

9: 92 percent / -78 °C / under dim red light

10: 98 percent / MnO₂ / CH₂Cl₂ / under dim red light

With 1H-imidazole; manganese(IV) oxide; sodium hydroxide; sodium tetrahydroborate; dipyridinium dichromate; dihydrogen peroxide; hydrogen cation; sodium hydride; diisobutylaluminium hydride; diisopinocampheylborane; In 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0040-4039(00)86036-0

Reference yield:

: 4436-51-5
1-hydroxymethyl-2,6,6-trimethylcyclohexa-1,3-diene

: 121468-86-8
(E)-4-[(S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,6,6-trimethyl-cyclohex-1-enyl]-but-3-en-2-one

Guidance literature:: Multi-step reaction with 9 steps

1: 98 percent / H⁽¹⁺⁾

2: 1.) (-)-diisopinocamphenyl borane, 2.) H₂O₂/NaOH

3: H⁽¹⁺⁾ / acetone

4: 50 percent / PDC / CH₂Cl₂; dioxane / under dim red light

5: 78 percent / NaH / under dim red light

6: 95 percent / imidazole / dimethylformamide / under dim red light

7: 70 percent / DIBAL / under dim red light

8: 92 percent / -78 °C / under dim red light

9: 98 percent / MnO₂ / CH₂Cl₂ / under dim red light

With 1H-imidazole; manganese(IV) oxide; sodium hydroxide; dipyridinium dichromate; dihydrogen peroxide; hydrogen cation; sodium hydride; diisobutylaluminium hydride; diisopinocampheylborane; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0040-4039(00)86036-0