HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967691Generated: November 2, 2026
HCID 86589658, compound → Phosphoglycolic Acid
https://huagongshe.com/reaction/967691
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86589658 | HCID 86589658 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Phosphoglycolic Acid | HCID 529 | — |
| Product | 2,2-Dimethoxypropane | HCID 6495 | — |
Reaction Steps
PGH is synthesized from tri(monocyclohexylammonium) 2-phosphoglycolate (Sigma-Aldrich Chemie GmBH, Germany), which is first converted into the free acid form using Dowex 50W-H+. Treatment of the 2-phosphoglycolic acid with 2,2-dimethoxypropane in methanol yielded the methyl ester 2PG, which is converted to PGH (Collins, K. D. (1974) J. Biol. Chem. 249:136-142). Purification of PGH to homogeneity is done on a DEAE Sephadex A-25 column using a 0-0.4 M lithium chloride gradient. Two consecutive purification columns are needed to obtain a product free of 2PG. PGH is isolated from LiCl by precipitation with barium salts (Lewis, D. J. & Lowe, G., (1977) Eu.r.J. Biochem. October, 17;80(1):119-33). The purity of the barium salt of PGH was confirmed by P NMR and H NMR and mass spectrometry. PGH solutions are prepared as described (Lewis & Lowe, 1977), and the concentration of dissolved PGH is determined spectrophotometrically (Collins, 1974).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06955890B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-63a95a87266c4376be7cdd5ba8ad3540 |
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| Source note | uspto-grants-2005_10 |
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