(R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-one

Base Information

Chemical Name:(R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-one
CAS No.:948582-50-1
Molecular Formula:C₃₉H₄₂O₄Si
Molecular Weight:602.846
Hs Code.:

Synonyms:(R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-one

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Chemical Property of (R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-one

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Technology Process of (R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-one

There total 10 articles about (R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-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: 67.0%

: 948582-48-7
(R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)prop-1-en-2-yl]-2-methylcyclohex-2-en-1-one

: 948582-50-1
(R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-one

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -10 ℃; for 18h;
DOI:10.1055/s-2007-983712

Reference yield:

: 870245-36-6
(R)-5-[3-(3-methoxyphenoxy)prop-1-en-2-yl]-2-methylcyclohex-2-en-1-one

: 948582-50-1
(R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-one

Guidance literature:: Multi-step reaction with 6 steps

1: 19 percent / BCl₃ / CH₂Cl₂ / 3 h / -50 - -20 °C

2: 18 percent / K₂CO₃ / dimethylformamide / 6 h / 60 °C

3: imidazole / dimethylformamide / 4 h / 20 °C

4: 76 percent / BCl₃ / CH₂Cl₂ / 1 h / -50 °C

5: 94 percent / KI; K₂CO₃ / dimethylformamide / 3 h / 20 °C

6: 67 percent / MCPBA / CH₂Cl₂ / 18 h / -10 °C

With 1H-imidazole; boron trichloride; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; potassium iodide; In dichloromethane; N,N-dimethyl-formamide; 1: Claisen rearrangement / 4: Claisen rearrangement;
DOI:10.1055/s-2007-983712

Reference yield:

: 870245-37-7
(R)-5-[3-(3-isopropoxyphenoxy)prop-1-en-2-yl]-2-methylcyclohex-2-en-1-one

: 948582-50-1
(R)-5-[3-(2-benzyloxy-4-tert-butyldiphenylsilyloxyphenyl)-1,2-epoxypropan-2-yl]-2-methylcyclohex-2-en-1-one

Guidance literature:: Multi-step reaction with 6 steps

1: 17 percent / BCl₃ / CH₂Cl₂ / 1 h / -50 °C

2: 18 percent / K₂CO₃ / dimethylformamide / 6 h / 60 °C

3: imidazole / dimethylformamide / 4 h / 20 °C

4: 76 percent / BCl₃ / CH₂Cl₂ / 1 h / -50 °C

5: 94 percent / KI; K₂CO₃ / dimethylformamide / 3 h / 20 °C

6: 67 percent / MCPBA / CH₂Cl₂ / 18 h / -10 °C

With 1H-imidazole; boron trichloride; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; potassium iodide; In dichloromethane; N,N-dimethyl-formamide; 1: Claisen rearrangement / 4: Claisen rearrangement;
DOI:10.1055/s-2007-983712