(Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid

Base Information

Chemical Name:(Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid
CAS No.:75626-58-3
Molecular Formula:C₂₁H₂₂N₂O₆
Molecular Weight:398.415
Hs Code.:

Synonyms:(Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid

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Chemical Property of (Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid

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Technology Process of (Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid

There total 6 articles about (Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid 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: 68.0%

: 110-87-2
3,4-dihydro-2H-pyran

: 75626-55-0
(Z)-4-<<(benzyloxy)carbonyl>amino>-α-(hydroxyimino)-phenylacetic acid

: 75626-58-3
(Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid

Guidance literature:: With toluene-4-sulfonic acid; In 1,4-dioxane; for 16h;
DOI:10.1021/jo00314a029

Reference yield: 59.0%

: 6723-30-4
O-2-tetrahydro-2H-pyranhydroxylamine

: 75626-51-6
4-<<(benzyloxy)carbonyl>amino>-α-oxophenylacetic acid

: 75626-58-3
(Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid

Guidance literature:: In pyridine; at 0 ℃; for 4h;
DOI:10.1021/jo00314a029

Reference yield:

: 72531-10-3
4-<<(benzyloxy)carbonyl>amino>acetophenone

: 75626-58-3
(Z)-4-<<(benzyloxy)carbonyl>amino>-α-<<(tetrahydro-2H-pyran-2-yl)oxy>imino>phenylacetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / selenium dioxide / 3 h / 100 °C

2: 59 percent / pyridine / 4 h / 0 °C

With selenium(IV) oxide; In pyridine;
DOI:10.1021/jo00314a029