N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide

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Chemical Name:N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide
CAS No.:147806-34-6
Molecular Formula:C₂₂H₂₉NO₃
Molecular Weight:355.477
Hs Code.:

Synonyms:N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide

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Chemical Property of N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide

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Technology Process of N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide

There total 9 articles about N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide 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: 97.0%

: 134031-39-3
(+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane

: 147806-34-6
N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 1h;

Reference yield:

: 930-30-3
cyclopent-2-enone

: 147806-34-6
N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide

Guidance literature:: Multi-step reaction with 7 steps

1: 1.) t-BuLi, 2.) 2-thienylCuCNLi, 3.) Me₃SiCl

2: 91 percent / 4-(dimethylamino)pyridine / CH₂Cl₂ / 12 h / Ambient temperature

3: 1.) 1,1,3,3-tetramethyl-1,3-diphenyl-disilazane, n-BuLi, 3.) Pd(PPh₃)4

4: 1.) MeLi, 2.) t-BuLi

5: t-BuOOH, Triton B / tetrahydrofuran / 2 h / -23 °C

6: 56 percent / tetrahydrofuran / 3 h / Ambient temperature

7: 97 percent / n-Bu₄NF / tetrahydrofuran / 1 h / 0 °C

With tert.-butylhydroperoxide; dmap; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; chloro-trimethyl-silane; 1,1,3,3-tetramethyl-1,3-diphenyldisilazane; tetrabutyl ammonium fluoride; methyllithium; tert.-butyl lithium; N-benzyl-trimethylammonium hydroxide; thien-2-yl(cyano)copper lithium; In tetrahydrofuran; dichloromethane;

Reference yield:

: 134031-36-0
(E)-4-<1-(((triisopropylsilyl)oxy)methyl)-1-propenyl>-1-<(N-methoxy-N-methylamino)carbonyl>cyclopentene

: 147806-34-6
N-(2-{1-[(1R,3R,5R)-3-((E)-1-Hydroxymethyl-propenyl)-6-oxa-bicyclo[3.1.0]hex-1-yl]-vinyl}-phenyl)-2,2-dimethyl-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) MeLi, 2.) t-BuLi

2: t-BuOOH, Triton B / tetrahydrofuran / 2 h / -23 °C

3: 56 percent / tetrahydrofuran / 3 h / Ambient temperature

4: 97 percent / n-Bu₄NF / tetrahydrofuran / 1 h / 0 °C

With tert.-butylhydroperoxide; tetrabutyl ammonium fluoride; methyllithium; tert.-butyl lithium; N-benzyl-trimethylammonium hydroxide; In tetrahydrofuran;