(R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol

Base Information

• Chemical Name: (R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol
• CAS No.: 152088-23-8
• Molecular Formula: C₂₁H₂₅NO₄
• Molecular Weight: 355.434
• Mol file: 152088-23-8.mol

Synonyms:(R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol

Chemical Property of (R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol

There total 2 articles about (R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol 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: 99.0%

(3R,5S,8aR)-5-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile (1025961-96-9) → (R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol (152088-23-8)

Guidance literature:

With sodium tetrahydroborate; In ethanol; for 12h; Heating;

DOI:10.1016/S0040-4020(01)89913-0

Reference yield:

(-)-2-cyano-6-phenyloxazolopiperidine (88056-92-2) → (R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol (152088-23-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) LDA / 1.) hexane, THF, -78 deg C, 45 min, 2.) THF, -78 deg C, 10 min

2: 99 percent / NaBH₄ / ethanol / 12 h / Heating

With sodium tetrahydroborate; lithium diisopropyl amide; In ethanol;

DOI:10.1016/S0040-4020(01)89913-0

Reference yield:

(R)-2-[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-2-phenyl-ethanol (152088-23-8) → (1R,3R,8aR)-1-Benzo[1,3]dioxol-5-yl-3-(3,4,5-trimethoxy-phenyl)-hexahydro-oxazolo[3,4-a]pyridine

Guidance literature:

Multi-step reaction with 2 steps

1: 99 percent / H₂ / 10percent Pd/C / ethanol / 12 h / 760 Torr

2: 80 percent / p-TsOH / toluene / 12 h / Heating

With hydrogen; toluene-4-sulfonic acid; palladium on activated charcoal; In ethanol; toluene;

DOI:10.1016/S0040-4020(01)89913-0

upstream raw materials:

(3R,5S,8aR)-5-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile

(-)-2-cyano-6-phenyloxazolopiperidine

Downstream raw materials:

[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-hydroxy-methyl)-piperidin-1-yl]-(3,4,5-trimethoxy-phenyl)-methanone

(1R,3R,8aR)-1-(6-Bromo-benzo[1,3]dioxol-5-yl)-3-(3,4,5-trimethoxy-phenyl)-hexahydro-oxazolo[3,4-a]pyridine

[(R)-2-((R)-Benzo[1,3]dioxol-5-yl-benzyloxy-methyl)-piperidin-1-yl]-(3,4,5-trimethoxy-phenyl)-methanone