-(RS)-isoleucinimino ethyl ether

Base Information

Chemical Name:-(RS)-isoleucinimino ethyl ether
CAS No.:132402-76-7
Molecular Formula:C₂₀H₃₁N₃O₅
Molecular Weight:393.483
Hs Code.:

<N-benzyloxycarbonyl-(S)-threonyl>-(RS)-isoleucinimino ethyl ether

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Suppliers and Price of -(RS)-isoleucinimino ethyl ether

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of -(RS)-isoleucinimino ethyl ether

Chemical Property:

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Technology Process of -(RS)-isoleucinimino ethyl ether

There total 3 articles about -(RS)-isoleucinimino ethyl ether 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:

: 96-17-3,57456-98-1
2-Methylbutyraldehyde

: 132402-76-7,132487-34-4
-(RS)-isoleucinimino ethyl ether

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / NH₄OAc / ethanol / 18 h / Ambient temperature

2: 94 percent / N-hydroxybenzotriazole, dicyclohexylcarbodiimide / CH₂Cl₂ / 18 h / Ambient temperature

3: HCl / diethyl ether / Ambient temperature

With hydrogenchloride; ammonium acetate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In diethyl ether; ethanol; dichloromethane;
DOI:10.1016/S0040-4020(01)81482-4

Reference yield:

: 128203-33-8
(RS)-isoleucinylnitrile

: 132402-76-7,132487-34-4
-(RS)-isoleucinimino ethyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / N-hydroxybenzotriazole, dicyclohexylcarbodiimide / CH₂Cl₂ / 18 h / Ambient temperature

2: HCl / diethyl ether / Ambient temperature

With hydrogenchloride; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In diethyl ether; dichloromethane;
DOI:10.1016/S0040-4020(01)81482-4