(2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic acid methyl ester

Base Information

Chemical Name:(2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic acid methyl ester
CAS No.:186758-22-5
Molecular Formula:C₁₀H₁₀F₂O₄
Molecular Weight:232.184
Hs Code.:

Synonyms:(2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic acid methyl ester

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Chemical Property of (2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic acid methyl ester

Chemical Property:

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Technology Process of (2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic acid methyl ester

There total 1 articles about (2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic 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: 71.0%

: 186758-21-4,166883-00-7
methyl (2E)-3-(2,4-difluorophenyl)prop-2-enoate

: 186758-22-5
(2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic acid methyl ester

Guidance literature:: With osmium(VIII) oxide; Hydroquinone 1,4-phthalazinediyl diether; potassium carbonate; potassium hexacyanoferrate(III); In water; tert-butyl alcohol; for 18h; Ambient temperature;
DOI:10.3987/com-96-s20

Reference yield:

: 186758-22-5
(2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic acid methyl ester

: 174729-94-3
methyl (2R,3S)-3-(2,4-difluorophenyl)-3-tert-butoxycarbonylamino-2-hydroxypropionate

Guidance literature:: Multi-step reaction with 5 steps

1: p-TsOH*H₂O / CH₂Cl₂ / 2.5 h / Ambient temperature

2: SnBr₂ / CH₂Cl₂ / -15 deg C, 1 h then 0 deg C, 2 h

3: 75 percent / sodium azide / dimethylformamide / 2.5 h / 40 °C

4: 73 percent / K₂CO₃ / methanol / 0.33 h / 0 °C

5: 91 percent / H₂ / Pd/C / ethyl acetate / 3.5 h / 760 Torr / Ambient temperature

With sodium azide; hydrogen; tin(II) bromide; potassium carbonate; toluene-4-sulfonic acid; palladium on activated charcoal; In methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.3987/com-96-s20

Reference yield:

: 186758-22-5
(2R,3S)-3-(2,4-Difluoro-phenyl)-2,3-dihydroxy-propionic acid methyl ester

: 174729-95-4
methyl (4S,5R)-3-tert-butoxycarbonyl-2,2-dimethyl-4-(2,4-difluorophenyl)-5-oxazolidinecarboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: p-TsOH*H₂O / CH₂Cl₂ / 2.5 h / Ambient temperature

2: SnBr₂ / CH₂Cl₂ / -15 deg C, 1 h then 0 deg C, 2 h

3: 75 percent / sodium azide / dimethylformamide / 2.5 h / 40 °C

4: 73 percent / K₂CO₃ / methanol / 0.33 h / 0 °C

5: 91 percent / H₂ / Pd/C / ethyl acetate / 3.5 h / 760 Torr / Ambient temperature

6: 74 percent / pyridinium p-toluenesulfonate / benzene / 90 °C

With sodium azide; hydrogen; pyridinium p-toluenesulfonate; tin(II) bromide; potassium carbonate; toluene-4-sulfonic acid; palladium on activated charcoal; In methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; benzene;
DOI:10.3987/com-96-s20