(3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol

Base Information

Chemical Name:(3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol
CAS No.:1027203-28-6
Molecular Formula:C₂₃H₄₄O₂S₂Si
Molecular Weight:444.819
Hs Code.:

(3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol

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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 (3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol

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Technology Process of (3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol

There total 7 articles about (3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol 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:

: 20549-46-6
(+)-neoisopulegol

: 1027203-28-6
(3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol

Guidance literature:: Multi-step reaction with 7 steps

1.1: 88 percent / t-BuOOH / VO(acac)2 / benzene / 20 °C

2.1: 79 percent / NaBH₃CN; BF₃*OEt₂; bromocresol green / tetrahydrofuran / 12 h / 20 °C

3.1: 84 percent / imidazole / dimethylformamide / 0.25 h / 20 °C

4.1: 88 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / 3.5 h / -65 - 20 °C

5.1: LHMDS / tetrahydrofuran / 0.83 h / -85 °C

5.2: HMPA / tetrahydrofuran / 1.92 h / -85 - 0 °C

6.1: LHMDS / tetrahydrofuran / 0.67 h / -82 °C

6.2: 1.74 g / tetrahydrofuran / 15 h / -55 - 20 °C

7.1: tetrahydrofuran / 1 h / 0 °C

With 1H-imidazole; tert.-butylhydroperoxide; oxalyl dichloride; boron trifluoride diethyl etherate; bromocresol green; sodium cyanoborohydride; dimethyl sulfoxide; triethylamine; lithium hexamethyldisilazane; bis(acetylacetonate)oxovanadium; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; benzene; 4.1: Swern oxidation;
DOI:10.1039/b102961b

Reference yield:

: 13834-16-7
(1R,2S,5R)-2-[(S)-2-hydroxy-1-methylethyl]-5-methylcyclohexan-1-ol

: 1027203-28-6
(3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: 84 percent / imidazole / dimethylformamide / 0.25 h / 20 °C

2.1: 88 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / 3.5 h / -65 - 20 °C

3.1: LHMDS / tetrahydrofuran / 0.83 h / -85 °C

3.2: HMPA / tetrahydrofuran / 1.92 h / -85 - 0 °C

4.1: LHMDS / tetrahydrofuran / 0.67 h / -82 °C

4.2: 1.74 g / tetrahydrofuran / 15 h / -55 - 20 °C

5.1: tetrahydrofuran / 1 h / 0 °C

With 1H-imidazole; oxalyl dichloride; dimethyl sulfoxide; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 2.1: Swern oxidation;
DOI:10.1039/b102961b

Reference yield:

: 181960-77-0
(2S,5R)-2-[(S)-2-(tert-butyldimethylsilyloxy)-1-methylethyl]-5-methylcyclohexan-1-ol

: 1027203-28-6
(3R,6S)-2-(Bis-methylsulfanyl-methylene)-6-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-3-methyl-1-(2-methyl-allyl)-cyclohexanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: 88 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / 3.5 h / -65 - 20 °C

2.1: LHMDS / tetrahydrofuran / 0.83 h / -85 °C

2.2: HMPA / tetrahydrofuran / 1.92 h / -85 - 0 °C

3.1: LHMDS / tetrahydrofuran / 0.67 h / -82 °C

3.2: 1.74 g / tetrahydrofuran / 15 h / -55 - 20 °C

4.1: tetrahydrofuran / 1 h / 0 °C

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; 1.1: Swern oxidation;
DOI:10.1039/b102961b