ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-1-carboxylate

Base Information

Chemical Name:ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-1-carboxylate
CAS No.:173396-48-0
Molecular Formula:C₂₃H₂₈O₆SeSi
Molecular Weight:507.517
Hs Code.:

Synonyms:ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-1-carboxylate

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Chemical Property of ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-1-carboxylate

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Technology Process of ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-1-carboxylate

There total 10 articles about ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-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: 96.0%

: 5707-04-0
Phenylselenyl chloride

: 173396-47-9
ethyl (1R,2S)-2,4-dihydroxy-5-methyl-2-(2-trimethylsilyl-3-furyl)-3-oxocyclohex-4-ene-1-carboxylate

: 173396-48-0
ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-1-carboxylate

Guidance literature:: With pyridine;
DOI:10.1039/c39950002519

Reference yield:

: 173396-45-7
ethyl (1R,2S,3R,5S)-2,3-dihydroxy-5-methyl-2-(2-trimethylsilyl-3-furyl)-4-oxocyclohexane-1-carboxylate

: 173396-48-0
ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / DMSO; (COCl)2; Et₃N / CH₂Cl₂ / -78 - 20 °C

2: 88 percent / pyridine / tetrahydrofuran / 0.08 h

With pyridine; oxalyl dichloride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; 1: Swern oxidation;
DOI:10.1039/b508675b

Reference yield:

: 173289-84-4
ethyl (1R,2S,3R,5S)-3-[(S)-O-(chloroacetyl)mandeloyloxy]-2-hydroxy-5-methyl-2-(2-trimethylsilyl-3-furyl)-4-oxocyclohexane-1-carboxylate

: 173396-48-0
ethyl (1R,2S,5R)-2-hydroxy-5-methyl-5-phenylselanyl-2-(2-trimethylsilyl-3-furyl)-3,4-dioxocyclohexane-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / K₂CO₃ / ethanol / 1 h / 0 °C

2: 90 percent / DMSO; (COCl)2; Et₃N / CH₂Cl₂ / -78 - 20 °C

3: 88 percent / pyridine / tetrahydrofuran / 0.08 h

With pyridine; oxalyl dichloride; potassium carbonate; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; 2: Swern oxidation;
DOI:10.1039/b508675b