(+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic acid

Base Information

Chemical Name:(+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic acid
CAS No.:183146-45-4
Molecular Formula:C₁₅H₁₉NO₆
Molecular Weight:309.319
Hs Code.:

Synonyms:(+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic acid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic acid

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Technology Process of (+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic acid

There total 3 articles about (+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic 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: 62.0%

: 183146-44-3
3-(3-Isopropyl-2-oxo-oxazolidin-5-ylmethoxy)-4-methoxy-benzoic acid methyl ester

: 183146-45-4
(+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic acid

Guidance literature:: With potassium hydroxide; In methanol; at 45 ℃; for 3h;

Reference yield:

: 6702-50-7
3-hydroxy-4-methoxybenzoate

: 183146-45-4
(+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaH / 1.) DMSO, 1 h, 2.) DMSO, 50 deg C, 20 h

2: 80 percent / LiCl / toluene / 72 h / 110 °C

3: 62 percent / 33percent aq. KOH / methanol / 3 h / 45 °C

With potassium hydroxide; sodium hydride; lithium chloride; In methanol; toluene;

Reference yield:

: 183146-43-2
4-Methoxy-3-oxiranylmethoxy-benzoic acid methyl ester

: 183146-45-4
(+/-)-3-[3-(1-methylethyl)-2-oxo-oxazolidin-5-ylmethoxy]-4-methoxybenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / LiCl / toluene / 72 h / 110 °C

2: 62 percent / 33percent aq. KOH / methanol / 3 h / 45 °C

With potassium hydroxide; lithium chloride; In methanol; toluene;