1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-ol

Base Information

Chemical Name:1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-ol
CAS No.:852119-03-0
Molecular Formula:C₂₅H₄₁NO₂Si
Molecular Weight:415.692
Hs Code.:

Synonyms:1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-ol

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Chemical Property of 1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-ol

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Technology Process of 1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-ol

There total 4 articles about 1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-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:

: 246245-91-0
(2R,6R)-1-(phenylmethyl)-2-(2-propen-1-yl)-2,6-piperidinedicarboxylic acid dimethyl ester

: 852119-03-0
1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 71 percent / LiAlH₄ / tetrahydrofuran / 5 h / 0 °C

2: 87 percent / imidazole; DMAP / CH₂Cl₂ / 0.67 h

3: DMSO; (COCl)2

4: tetrahydrofuran / 0.5 h / -20 °C

With 1H-imidazole; dmap; lithium aluminium tetrahydride; oxalyl dichloride; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; 3: Swern oxidation;
DOI:10.1016/j.tetlet.2005.02.133

Reference yield:

: 820967-79-1
(2R,6R)-1-(phenylmethyl)-2-(2-propen-1-yl)-2,6-piperidinedimethanol

: 852119-03-0
1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / imidazole; DMAP / CH₂Cl₂ / 0.67 h

2: DMSO; (COCl)2

3: tetrahydrofuran / 0.5 h / -20 °C

With 1H-imidazole; dmap; oxalyl dichloride; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; 2: Swern oxidation;
DOI:10.1016/j.tetlet.2005.02.133

Reference yield:

: 852118-99-1
(2R,6R)-6-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-1-(phenylmethyl)-2-(2-propen-1-yl)-2-piperidinemethanol

: 852119-03-0
1-[(2R,6R)-2-Allyl-1-benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-piperidin-2-yl]-prop-2-en-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: DMSO; (COCl)2

2: tetrahydrofuran / 0.5 h / -20 °C

With oxalyl dichloride; dimethyl sulfoxide; In tetrahydrofuran; 1: Swern oxidation;
DOI:10.1016/j.tetlet.2005.02.133