(R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

Base Information

Chemical Name:(R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one
CAS No.:204577-68-4
Molecular Formula:C₁₉H₂₆O₃
Molecular Weight:302.414
Hs Code.:

Synonyms:(R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

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Chemical Property of (R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

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Technology Process of (R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

There total 8 articles about (R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one 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: 67.0%

: 100-52-7
benzaldehyde

: 204577-66-2
1-(2-hydroxy-1,7,7-trimethylbicyclo[2.2.1]hept-endo-2-yl)ethanone

: (S)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

: 204577-68-4
(R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

Guidance literature:: 1-(2-hydroxy-1,7,7-trimethylbicyclo[2.2.1]hept-endo-2-yl)ethanone; With lithium chloride; lithium diisopropyl amide; In tetrahydrofuran; hexane; at -78 ℃; for 1h;

benzaldehyde; In tetrahydrofuran; hexane; at -78 ℃;
DOI:10.1021/jo990865z

Reference yield:

: 1075216-42-0
2-ethinyl-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

: 204577-68-4
(R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: 17.6 g / red mercuric oxide; concentrated sulfuric acid; water / acetone / 1.75 h / 60 °C

2.1: 100 percent / trifluoromethanesulfonic acid / 1 h / 20 °C

3.1: lithium diisopropylamide / tetrahydrofuran; hexane / 1 h / -78 °C

3.2: 80 percent / tetrahydrofuran; hexane / -78 °C

4.1: aq. HCl / methanol / 3 h / 20 °C

With hydrogenchloride; trifluorormethanesulfonic acid; sulfuric acid; water; mercury(II) oxide; lithium diisopropyl amide; In tetrahydrofuran; methanol; hexane; acetone; 1.1: hydration / 2.1: silylation / 3.1: Metallation / 3.2: Addition / 4.1: desilylation;
DOI:10.1021/jo990865z

Reference yield:

: 3-Hydroxy-3-phenyl-1-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-propan-1-one

: (S)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

: 204577-68-4
(R)-3-Hydroxy-1-((1R,2R,4R)-2-hydroxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-3-phenyl-propan-1-one

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; for 0.0833333h; Yields of byproduct given. Title compound not separated from byproducts; Ambient temperature;
DOI:10.1002/(sici)1521-3773(19980202)37:1/2<180::aid-anie180>3.0.co;2-4