methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate

Base Information

Chemical Name:methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate
CAS No.:111515-87-8
Molecular Formula:C₁₀H₁₅NO₅
Molecular Weight:229.233
Hs Code.:

Synonyms:methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate

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Chemical Property of methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate

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Technology Process of methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate

There total 4 articles about methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate 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: 92.0%

: 111515-77-6
(1R,2S,5S)-2-<(methoxycarbonyl)amino>-7-oxo-6-oxabicyclo<3.2.1>oct-3-ene

: 124-41-4
sodium methylate

: 111515-87-8
methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate

Guidance literature:: In methanol; at -10 ℃; for 1h;
DOI:10.1021/jo00291a014

Reference yield:

: 124287-85-0
(1R,2S,4S,5S)-2-<(methoxycarbonyl)amino>-4-iodo-7-oxo-6-oxabicyclo<3.2.1>octane

: 111515-87-8
methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / DBU / benzene / 3 h / Heating

2: 92 percent / methanol / 1 h / -10 °C

With 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; benzene;
DOI:10.1021/jo00291a014

Reference yield:

: 124287-84-9
(1R,6S)-6-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylic acid

: 111515-87-8
methyl (1R,2S,5S)-5-hydroxy-2-<(methoxycarbonyl)amino>cyclohex-3-enecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / I₂, KI, NaHCO₃ / CH₂Cl₂; H₂O / 20 h / Ambient temperature

2: 94 percent / DBU / benzene / 3 h / Heating

3: 92 percent / methanol / 1 h / -10 °C

With iodine; sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; potassium iodide; In methanol; dichloromethane; water; benzene;
DOI:10.1021/jo00291a014