methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate

Base Information

Chemical Name:methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate
CAS No.:1450734-58-3
Molecular Formula:C₁₇H₂₅NO₆
Molecular Weight:339.389
Hs Code.:

Synonyms:methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate

Suppliers and Price of methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate

Supply Marketing:

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

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Chemical Property of methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate

There total 5 articles about methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate 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%

: 1450734-54-9
4-methoxybenzyl N-phenyl-2,2,2-trifluoroacetimidate

: 2766-43-0
N-tert-butyloxycarbonyl-L-serine methyl ester

: 1450734-58-3
methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate

Guidance literature:: With bismuth(lll) trifluoromethanesulfonate; In toluene; at 20 ℃; for 0.5h; Molecular sieve; Inert atmosphere;
DOI:10.1016/j.tetlet.2013.07.066

Reference yield: 80.0%

: 100867-01-4
(4-methoxybenzyl)(4-nitrophenyl)sulfane

: 2766-43-0
N-tert-butyloxycarbonyl-L-serine methyl ester

: 1450734-58-3
methyl (S)-3-(4-methoxybenzyl)-2-(N-tert-butyloxycarbonyl)aminopropanoate

Guidance literature:: With rhodium (II) octanoate dimer; 2,6-di-tert-butyl-4-methylpyridinium trifluoromethanesulfonate; methyl 2-(4-chlorophenyl)-2-diazoacetate; In dichloromethane; at 0 ℃; for 0.5h; Molecular sieve;
DOI:10.1016/j.cclet.2021.06.069