4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine

Base Information

Chemical Name:4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine
CAS No.:160195-21-1
Molecular Formula:C₂₁H₂₇NO
Molecular Weight:309.451
Hs Code.:

Synonyms:4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine

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Chemical Property of 4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine

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Technology Process of 4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine

There total 1 articles about 4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine 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: 84.0%

: 626-61-9
4-Chloropyridine

: 65253-04-5
(-)-8-phenylmenthol

: 160195-21-1
4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine

Guidance literature:: With potassium tert-butylate; In dimethyl sulfoxide; at 25 ℃; for 24h;
DOI:10.1016/0040-4039(94)85309-6

Reference yield: 58.0%

: 13154-24-0
triisopropylsilyl chloride

: 160195-21-1
4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine

: 160195-24-4
4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-3-triisopropylsilanyl-pyridine

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; Heating;
DOI:10.1016/0040-4039(94)85309-6

Reference yield:

: 160195-21-1
4-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-pyridine

: (R)-2-Methyl-4-oxo-5-triisopropylsilanyl-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / LDA / tetrahydrofuran / Heating

3: 68 percent / oxalic acid / methanol / Heating

With oxalic acid; lithium diisopropyl amide; In tetrahydrofuran; methanol;
DOI:10.1016/0040-4039(94)85309-6