<1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-penten-5-ol

Base Information

Chemical Name:<1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-penten-5-ol
CAS No.:136358-58-2
Molecular Formula:C₃₅H₆₅NO₇Si
Molecular Weight:639.989
Hs Code.:

<1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-penten-5-ol

Synonyms:<1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-penten-5-ol

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Chemical Property of <1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-penten-5-ol

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Technology Process of <1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-penten-5-ol

There total 8 articles about <1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-penten-5-ol 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: 80.5%

: 136358-57-1
<1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-5-<(4-methoxybenzyl)oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-pentene

: 136358-58-2
<1(1R,3R,4R),1E,3(2S),3S>-3-<<<-N-(tert-butoxycarbonyl)piperidin-2-yl>carbonyl>oxy>-1-<3-methoxy-4-<(triisopropylsilyl)oxy>cyclohex-1-yl>-2,4,4-trimethyl-1-penten-5-ol

Guidance literature:: With water; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane;

Reference yield: 52.0%

: 136358-57-1
(S)-Piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-[(E)-(S)-1-[2-(4-methoxy-benzyloxy)-1,1-dimethyl-ethyl]-3-((1R,3R,4R)-3-methoxy-4-triisopropylsilanyloxy-cyclohexyl)-2-methyl-allyl] ester

: 136358-58-2
(S)-Piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-[(E)-(S)-1-(2-hydroxy-1,1-dimethyl-ethyl)-3-((1R,3R,4R)-3-methoxy-4-triisopropylsilanyloxy-cyclohexyl)-2-methyl-allyl] ester

Guidance literature:: With water; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane;

Reference yield:

: 92156-87-1
2,2-dimethyl-3-(4-methoxyphenylmethoxy)propionaldehyde

: 136358-58-2
(S)-Piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-[(E)-(S)-1-(2-hydroxy-1,1-dimethyl-ethyl)-3-((1R,3R,4R)-3-methoxy-4-triisopropylsilanyloxy-cyclohexyl)-2-methyl-allyl] ester

Guidance literature:: Multi-step reaction with 3 steps

2: 75 percent / diisopropylcarbodiimide (DIPCDI), 4-pyrrolidinopyridine

3: 52 percent / DDQ, H₂O / CH₂Cl₂

With water; 4-pyrrolidin-1-ylpyridine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; diisopropyl-carbodiimide; In dichloromethane;