(4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester

Base Information

Chemical Name:(4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester
CAS No.:175408-52-3
Molecular Formula:C₁₅H₂₀NO₅P
Molecular Weight:325.301
Hs Code.:

Synonyms:(4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester

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Chemical Property of (4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester

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Technology Process of (4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester

There total 1 articles about (4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl 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:

: 27772-80-1
4-methyl-5-phenyl-3-hydroxyisoxazole

: 114108-84-8
diethyl <<(methylsulfonyl)oxy>methyl>phosphonate

: 175408-52-3
(4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester

Guidance literature:: With potassium carbonate; Yield given. Multistep reaction; 1.) DMF, 80 deg C, 30 min, 2.) DMF, 80 deg C, 3.5 h;
DOI:10.1021/jm950826p

Reference yield: 100.0%

: 175408-52-3
(4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester

: 175408-56-7
(4-Bromomethyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester

Guidance literature:: With N-Bromosuccinimide; Perbenzoic acid; In tetrachloromethane; for 8h; Heating;
DOI:10.1021/jm950826p

Reference yield:

: 175408-52-3
(4-Methyl-5-phenyl-isoxazol-3-yloxymethyl)-phosphonic acid diethyl ester

: 2-Amino-3-(5-phenyl-3-phosphonomethoxy-isoxazol-4-yl)-propionic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / NBS, benzoyl peroxide / CCl₄ / 8 h / Heating

2: 1.) potassium tert-butoxide / 1.) N-methylpyrrolidone, RT, 30 min, 2.) N-methylpyrrolidone, 1 h

3: 99 percent / trimethylsilyl bromide / acetonitrile / 24 h / Ambient temperature

4: 63 percent / 1 M HCl / Heating

With hydrogenchloride; N-Bromosuccinimide; Perbenzoic acid; trimethylsilyl bromide; potassium tert-butylate; In tetrachloromethane; acetonitrile;
DOI:10.1021/jm950826p