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HRID 1402641作成日:2026年10月27日

Disodium 2,3-dihydroxybutanedioate → 2,3-Dihydroxybutanedioic Acid

https://huagongshe.com/reaction/1402641

反応式

関与物質

役割名称HCID仕込み量
反応物Disodium 2,3-dihydroxybutanedioateHCID 13355—
反応物Sodium HydroxideHCID 14798—
反応物TartrateHCID 119400—
反応物Sodium TartrateHCID 162637—
反応物L-Tartaric acidHCID 444305—
生成物2,3-Dihydroxybutanedioic AcidHCID 875—
生成物Sodium HydroxideHCID 14798—
生成物Sodium 3-carboxy-2,3-dihydroxypropanoateHCID 23690454—

反応手順

L(+)-tartaric acid disodium salt, also denoted as bisodium L-tartrate, is commercially available, e.g. from Sigma-Aldrich (CAS Number 6106-24-7). It is noted that instead of using L(+)-tartaric acid disodium salt, it is also possible to use L(+)-tartaric acid (commercially available from e.g. Sigma-Aldrich, CAS Number 87-69-4) and prepare the L(+)-tartaric acid disodium salt in situ, by addition of additional NaOH. The same holds for the other potential starting material, DL-tartaric acid disodium salt: it may be purchased from e.g. Sigma-Aldrich or produced in situ from DL-tartaric acid (CAS Number 133-37-9) or DL-tartaric acid monosodium salt and NaOH. In fact any tartaric acid source, containing D, L, meso in any proportion and in the acidic or salt form can be used for this process. D-tartaric acid can also be used as starting material, but this is less preferred because it is relatively expensive. The use of L-tartaric acid disodium salt (either produced in situ by addition of NaOH or used as such) is preferred because these starting materials are relatively cheap and the process to prepare a composition with between 55 and 90% by weight of meso-tartaric acid is faster than when a mixture of D- and L-tartaric acid is used as starting material. Obviously, it is also possible to use a mixture of D-, L-, and meso-tartaric acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08911796B2
出典データセットuspto-grants-2014_12
ORD IDord-fbb400d9cb2d45bc8931e8f7c6f6330d
出典メモuspto-grants-2014_12