HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437862Generated: October 29, 2026
Hydrochloric Acid → HCID 131710826, compound
https://huagongshe.com/reaction/437862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 131710827 | HCID 131710827 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131710826 | HCID 131710826 | — |
Reaction Steps
Trisodium 3-acetoxymethyl-7β-(2-[3-thienyl]- 2-carboxyacetamido)-3-cephem-4-phosphonate (1 g.) is dissolved in 100 ml. of a solution of citrus acetyl esterase (J.D.A. Jeffery, et. al., Biochem. J. (1961) 81, 591). The pH is adjusted to 6.6 and the mixture is maintained at 30° C. 1 N NaOH is added dropwise to maintain the pH at 6.6 as the reaction proceeds and the reaction is continued until no further pH change occurs. 10 g. Nacl is added and the mixture is layered with 50 ml. EtOAc, the pH is adjusted to 2.1 with HCl and the mixture is stirred vigorously. The EtOAc layer is separated and washed once with water and then layered with water and stirred and the pH of the aqueous phase is adjusted to 5.9 with 6 N NaOH. The aqueous layer is separated and freeze-dried to give trisodium 3-hydroxymethyl-7β-(2-[3-thienyl]-2-carboxyacetamido)-3-cephem-4-phosphonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04032521 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-84487e50decc4375bfe62a632210b8c1 |
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| Source note | uspto-grants-1977_06 |
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