(2S,4S)-2-p-Tolyl-4-trimethylsilanyl-cyclopentanone

Base Information

Chemical Name:(2S,4S)-2-p-Tolyl-4-trimethylsilanyl-cyclopentanone
CAS No.:131110-72-0
Molecular Formula:C₁₅H₂₂OSi
Molecular Weight:246.425
Hs Code.:

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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 (2S,4S)-2-p-Tolyl-4-trimethylsilanyl-cyclopentanone

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Technology Process of (2S,4S)-2-p-Tolyl-4-trimethylsilanyl-cyclopentanone

There total 8 articles about (2S,4S)-2-p-Tolyl-4-trimethylsilanyl-cyclopentanone 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:

: 56917-71-6
5-trimethylsilyl-2-cyclohexanone

: 131110-72-0
2-p-Tolyl-4-trimethylsilanyl-cyclopentanone

Guidance literature:: Multi-step reaction with 4 steps

2: 68 percent / 35percent H₂O₂, benzyltrimethylammonium hydroxide / ethanol / 0.25 h / Ambient temperature

3: BF₃*Et₂O

4: NaOH

With sodium hydroxide; boron trifluoride diethyl etherate; dihydrogen peroxide; N-benzyl-trimethylammonium hydroxide; In ethanol;

Reference yield:

: 116215-94-2
(R)-(-)-5-trimethylsilyl-2-cyclohexenone

: 131110-72-0
(2S,4S)-2-p-Tolyl-4-trimethylsilanyl-cyclopentanone

Guidance literature:: Multi-step reaction with 4 steps

2: 35percent H₂O₂, benzyltrimethylammonium hydroxide / ethanol

3: BF₃*Et₂O

4: NaOH

With sodium hydroxide; boron trifluoride diethyl etherate; dihydrogen peroxide; N-benzyl-trimethylammonium hydroxide; In ethanol;

Reference yield:

: 131110-62-8
3-p-Tolyl-5-trimethylsilanyl-cyclohex-2-enone

: 131110-72-0
2-p-Tolyl-4-trimethylsilanyl-cyclopentanone

Guidance literature:: Multi-step reaction with 3 steps

1: 68 percent / 35percent H₂O₂, benzyltrimethylammonium hydroxide / ethanol / 0.25 h / Ambient temperature

2: BF₃*Et₂O

3: NaOH

With sodium hydroxide; boron trifluoride diethyl etherate; dihydrogen peroxide; N-benzyl-trimethylammonium hydroxide; In ethanol;