(1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol

Base Information

Chemical Name:(1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol
CAS No.:740800-49-1
Molecular Formula:C₂₁H₃₆O₂Si
Molecular Weight:348.601
Hs Code.:

Synonyms:(1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol

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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 (1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol

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Technology Process of (1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol

There total 3 articles about (1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol 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%

: (1S,2S,4R)-4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentanecarboxylic acid ethyl ester

: 740800-49-1
(1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; at 0 - 20 ℃;
DOI:10.1016/j.tet.2004.05.037

Reference yield:

: (1R,2R,4S)-4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-2-p-tolyl-cyclopentanecarboxylic acid ethyl ester

: 740800-49-1
(1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: LDA; HMPA / tetrahydrofuran; diethyl ether; hexane / -90 °C

1.2: tetrahydrofuran; diethyl ether; hexane / -90 - 0 °C

2.1: 95 percent / LiAlH₄ / diethyl ether / 0 - 20 °C

With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium aluminium tetrahydride; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; hexane;
DOI:10.1016/j.tet.2004.05.037

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 740800-49-1
(1S,2S,4R)-[4-(tert-butyl-dimethyl-silanyloxy)-1,2-dimethyl-2-p-tolyl-cyclopentyl]methanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: imidazole / dimethylformamide / 20 °C

2.1: LDA; HMPA / tetrahydrofuran; diethyl ether; hexane / -90 °C

2.2: tetrahydrofuran; diethyl ether; hexane / -90 - 0 °C

3.1: 95 percent / LiAlH₄ / diethyl ether / 0 - 20 °C

With 1H-imidazole; N,N,N,N,N,N-hexamethylphosphoric triamide; lithium aluminium tetrahydride; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; hexane; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2004.05.037