1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane

Base Information

Chemical Name:1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane
CAS No.:126087-74-9
Molecular Formula:C₁₉H₂₇NOSSi
Molecular Weight:345.581
Hs Code.:

Synonyms:1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane

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Technology Process of 1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane

There total 1 articles about 1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane 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: 95.0%

: 7677-24-9
trimethylsilyl cyanide

: 116512-71-1
6,6-dimethyl-2-phenylthiomethylen-cyclohexanone

: 126087-74-9
1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane

Guidance literature:: With zinc(II) iodide; In dichloromethane; for 1h; Ambient temperature;

Reference yield: 80.0%

: 126087-74-9
1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane

: 126087-75-0
6,6-dimethyl-2-phenylthiomethyl-1-cyclohexencarboxaldehyde

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; toluene; at -80 ℃; for 0.5h;

Reference yield:

: 126087-74-9
1-cyano-6,6-dimethyl-2-phenylthiomethylene-1-trimethylsilyloxy-cyclohexane

: 126087-76-1
4,4-dimethyl-1-phenylthio-4,5,6,7-tetrahydroisobenzofuran

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / DIBAL / toluene; CH₂Cl₂ / 0.5 h / -80 °C

2: sodiumperiodate / acetonitrile; methanol; H₂O / 36 h / Ambient temperature

3: 1.) 2,6-lutidine, trifluoroacetic anhydride, 2.) aq. KOH / 1.) CH₂Cl₂, room tempetature, 1 h, 2.) 30 min

With 2,6-dimethylpyridine; potassium hydroxide; sodium periodate; diisobutylaluminium hydride; trifluoroacetic anhydride; In methanol; dichloromethane; water; toluene; acetonitrile;