tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate
CAS No.:1415971-14-0
Molecular Formula:C₂₅H₃₇NO₅
Molecular Weight:431.572
Hs Code.:

Synonyms:tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate

Suppliers and Price of tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate

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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 tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate

There total 1 articles about tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate 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: 75.0%

: 4335-77-7,20585-34-6,20585-39-1,50896-04-3
cyclohexylmandelic acid

: 158407-04-6
tert-butyl 4-(bromomethyl)piperidine-1-carboxylate

: 1415971-14-0
tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 72h;

Reference yield:

: 1415971-14-0
tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate

: 1415971-15-1
(piperidin-4-yl)methyl 2-cyclohexyl-2-hydroxy-2-phenylacetate hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; dichloromethane; at 20 ℃; for 3h;

Reference yield:

: 1415971-14-0
tert-butyl 4-((2-cyclohexyl-2-hydroxy-2-phenylacetyloxy)methyl)piperidine-1-carboxylate

: 1415971-16-2
(1-(9-(1,3-dioxolan-2-yl)nonyl)piperidin-4-yl)methyl 2-cyclohexyl-2-hydroxy-2-phenylacetate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / dichloromethane; 1,4-dioxane / 3 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 17 h / 60 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; acetonitrile;