<4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl ester

Base Information

Chemical Name:<4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl ester
CAS No.:152565-35-0
Molecular Formula:C₁₁H₉F₃N₂O₃
Molecular Weight:274.199
Hs Code.:

Synonyms:<4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl ester

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Chemical Property of <4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl ester

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Technology Process of <4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl ester

There total 9 articles about <4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl 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: 63.0%

: 96-32-2
bromoacetic acid methyl ester

: 156824-51-0
3-(4-hydroxyphenyl)-3-trifluoromethyldiazirine

: 152565-35-0
<4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl ester

Guidance literature:: With cesium fluoride; In acetonitrile; at 0 ℃; for 3h;
DOI:10.1021/jo00081a017

Reference yield:

: 891501-19-2
3-(4-Methoxyphenyl)-3-(trifluoromethyl)-3H-diazirine

: 152565-35-0
<4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 26 percent / (CH₃)SiI / pentane / 65 h / Ambient temperature

2: 63 percent / CsF / acetonitrile / 3 h / 0 °C

With (CH₃)SiI; cesium fluoride; In acetonitrile; pentane;
DOI:10.1021/jo00081a017

Reference yield:

: 106-41-2
4-bromo-phenol

: 152565-35-0
<4-<3-(Trifluoromethyl)-3H-diazirin-3-yl>phenoxy>acetic acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 1.) KOH / 1.) methanol, 2.) acetonitrile, RT, 30 min

2: 1.) Mg / 1.) THF, 2.) THF

3: 98 percent / NH₂OH*HCl / ethanol; pyridine / 4 h / 60 °C

4: Et₃N, N,N-dimethylaminopyridine / CH₂Cl₂ / 0.5 h / Ambient temperature

5: NH₃ (liq.) / CH₂Cl₂ / 12 h / Ambient temperature

6: 85 percent / tert-butyl hypochlorite, Et₃N / 2-methyl-propan-2-ol; ethanol / 0.5 h / 0 °C

7: acetic acid, 1N aq. HCl / 12 h / Ambient temperature

8: CsF / acetonitrile / 3 h / 0 °C

With hydrogenchloride; dmap; potassium hydroxide; tert-butylhypochlorite; hydroxylamine hydrochloride; ammonia; magnesium; acetic acid; triethylamine; cesium fluoride; In pyridine; ethanol; dichloromethane; acetonitrile; tert-butyl alcohol;
DOI:10.1248/cpb.42.826