HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707188Generated: November 1, 2026
Phosphate → 7beta-(2-Hydroxyimino-2-phenylacetamido)-3-hydroxymethyl-ceph-3-em-4-carboxylic acid sodium salt
https://huagongshe.com/reaction/1707188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 88767746 | HCID 88767746 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7beta-(2-Hydroxyimino-2-phenylacetamido)-3-hydroxymethyl-ceph-3-em-4-carboxylic acid sodium salt | HCID 131710754 | — |
Reaction Steps
To 3-acetoxymethyl-7β-(2-hydroxyimino-2-phenylacetamido)ceph-3-em-4-carboxylic acid (syn-isomer) (5.0 g) was added sufficient saturated sodium bicarbonate solution to bring the pH to 7.0, during which time solution occurred. To this solution was added water (300 ml.) and defatted wheat germ (35 g.), and the suspension stirred vigorously whilst the pH was maintained at between 6.7 and 6.9 by frequent additions of 2 N-sodium hydroxide. After addition of ca. 6 ml, the pH remained constant at 6.9. The mixture was poured into acetone (400 ml.), filtered (kieselguhr), and the filtrate evaporated under reduced pressure to remove acetone, then refiltered (kieselguhr). The filtrate was washed with ethyl acetate, and the pH adjusted to 2.8. The aqueous phase was extracted with ethyl acetate, and the extracts were stirred with water (ca. 300 ml.) and the pH brought up to 7.0 with 2 N sodium hydroxide. Th phases were separated and the aqueous phase washed twice with ethyl acetate, once with ether, evaporated under reduced pressure to remove residual solvents, and freeze-dried. This gave the title acid (1.5 g: 31%), [α]D +93° (c 1.0, DMSO), λmax. (pH 6 phosphate buffer) 252 nm (ε 12,800), νmax. (Nujol) 1750 (β-lactam), 1650 and 1530 cm.-1 (amide), τ (DMSO-d6) values include 2.3 to 2.6 (multiplet; aromatic protons), 5.72 and 6.05 [two doublets (branches of a quartet), J 13 Hz; CH2OH], 6.44 and 6.68 [two doublets (branches of a quartet), J 18 Hz; C-2CH2 ].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04209616 |
|---|
| Source dataset | uspto-grants-1980_06 |
|---|
| ORD ID | ord-3d06ab6bbc734f688c657a14cc4110cc |
|---|
| Source note | uspto-grants-1980_06 |
|---|