2-Tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester

Base Information

Chemical Name:2-Tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester
CAS No.:38308-93-9
Molecular Formula:C₁₆H₂₃NO₅
Molecular Weight:309.362
Hs Code.:
DSSTox Substance ID:DTXSID401186930

Synonyms:38308-93-9;SCHEMBL1094804;YQTGYJUMDNISEP-UHFFFAOYSA-N;2-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester;DTXSID401186930;FT-0772908;N-[(1,1-Dimethylethoxy)carbonyl]homoserine phenylmethyl ester

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Chemical Property of 2-Tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:9
Exact Mass:309.15762283
Heavy Atom Count:22
Complexity:358

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CCO)C(=O)OCC1=CC=CC=C1

Technology Process of 2-Tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester

There total 4 articles about 2-Tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester 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: 93.0%

: 34619-03-9
tert-butyldicarbonate

: 100-39-0
benzyl bromide

: 6305-38-0
α-amino-γ-butyrolactone hydrobromide

: 38308-93-9
2-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester

Guidance literature:: With sodium hydroxide; ammonium chloride; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: DL-homoserine hydrobromide

: 24424-99-5
di-tert-butyl dicarbonate

: 100-39-0
benzyl bromide

: 38308-93-9
2-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester

Guidance literature:: DL-homoserine hydrobromide; With sodium hydroxide; caesium carbonate; for 0.0833333h;

di-tert-butyl dicarbonate; In 1,4-dioxane; at 0 - 20 ℃; for 6h;

benzyl bromide; In N,N-dimethyl-formamide; for 16h;
DOI:10.1021/jm060482a