(5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine

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Chemical Name:(5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine
CAS No.:131120-96-2
Molecular Formula:C₂₇H₂₁Cl₄N₃O
Molecular Weight:545.295
Hs Code.:

Synonyms:(5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine

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Chemical Property of (5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine

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Technology Process of (5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine

There total 3 articles about (5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine 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: 55.0%

: 131120-95-1
N-<3-(1-trityl-1H-imidazol-4-yl)prop-2-enyl>-trichloroacetamide trans

: 131120-96-2
(5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine

Guidance literature:: With calcium hypochlorite; carbon dioxide; In dichloromethane; at 10 ℃; for 1h;
DOI:10.1016/S0040-4039(00)97492-6

Reference yield:

: 127798-61-2
1-(1-trityl-1H-imidazol-4-yl)-prop-2-en-1-ol

: 131120-96-2
(5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine

Guidance literature:: Multi-step reaction with 2 steps

1: 22 percent / DBU / CH₂Cl₂ / 24 h / 20 °C

2: 55 percent / a.Ca(OCl)2, CO₂ / CH₂Cl₂ / 1 h / 10 °C

With calcium hypochlorite; carbon dioxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane;
DOI:10.1016/S0040-4039(00)97492-6

Reference yield:

: 33016-47-6
(1-tritylimidazol-4-yl)carboxaldehyde

: 131120-96-2
(5S,6R)-5-Chloro-2-trichloromethyl-6-(1-trityl-1H-imidazol-4-yl)-5,6-dihydro-4H-[1,3]oxazine

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / tetrahydrofuran / -10 °C

2: 22 percent / DBU / CH₂Cl₂ / 24 h / 20 °C

3: 55 percent / a.Ca(OCl)2, CO₂ / CH₂Cl₂ / 1 h / 10 °C

With calcium hypochlorite; carbon dioxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4039(00)97492-6