(9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate

Base Information

Chemical Name:(9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate
CAS No.:1596118-28-3
Molecular Formula:C₁₉H₂₀N₂O₄
Molecular Weight:340.379
Hs Code.:

Synonyms:(9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate

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Chemical Property of (9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate

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Technology Process of (9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate

There total 1 articles about (9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate 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: 75.0%

: 94744-50-0
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid

: 1596118-28-3
(9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate

Guidance literature:: N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid; With dmap; ethyl 2-cyano-2-(4-nitrophenylsulfonyloxyimino)acetate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 0.5h;

With hydroxylamine hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jo4026429

Reference yield: 81.0%

: 2577-90-4
methyl (2S)-2-amino-3-phenylpropanoate

: 1596118-28-3
(9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate

: 1596118-36-3
C₂₉H₃₁N₃O₅

Guidance literature:: (9H-fluoren-9-yl)methyl (1-(hydroxyamino)-2-methyl-1-oxopropan-2-yl)carbamate; With ethyl 2-cyano-2-(4-nitrophenylsulfonyloxyimino)acetate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 0 ℃; for 1.5h;

methyl (2S)-2-amino-3-phenylpropanoate; In tetrahydrofuran; at 20 ℃; for 4h;
DOI:10.1021/jo4026429