1-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene

Base Information

Chemical Name:1-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene
CAS No.:120173-34-4
Molecular Formula:C₂₁H₃₄O
Molecular Weight:302.5
Hs Code.:

Synonyms:1-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene

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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-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene

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Technology Process of 1-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene

There total 1 articles about 1-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene 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:

: 51991-28-7
1-bromo-4-neopentylbenzene

: 120520-42-5
(1R,3S)-1,2,2,3-tetramethyl-1-cyclopentanecarboxaldehyde

: 120173-34-4
1-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene

Guidance literature:: With magnesium; Yield given. Multistep reaction; 1.) THF, 10 min, reflux; 2.) THF, 1 h, reflux;

Reference yield: 100.0%

: 120173-34-4
1-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene

: 120173-37-7
1-<(ξ)-chloro<(1S,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene

Guidance literature:: With pyridine; thionyl chloride; In diethyl ether; for 2h; Ambient temperature;

Reference yield:

: 120173-34-4
1-<(S)-hydroxy<(1R,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>-4-neopentylbenzene

: 120173-40-2
4-neopentyl-1-<<(1S,3S)-1,2,2,3-tetramethylcyclopentyl>methyl>benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / SOCl₂, pyridine / diethyl ether / 2 h / Ambient temperature

2: 55 percent / tert-butyl alcohol, Li / tetrahydrofuran / 2 h / Heating

With pyridine; thionyl chloride; lithium; tert-butyl alcohol; In tetrahydrofuran; diethyl ether;