HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902803Generated: October 31, 2026
Sodium Bicarbonate → HCID 53643909, compound
https://huagongshe.com/reaction/1902803
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 70554645 | HCID 70554645 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53643909 | HCID 53643909 | 93.3% |
Reaction Steps
A mixture of 3-(2-acetoxy-vinyl)-2-benzhydryloxycarbonyl-7-tert.-butoxycarbonylamino-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (E-form) (1.65 g) (obtained as described above in Example 5), p-toluenesulphonic acid monohydrate (1.14 g) and acetonitrile (50 cc) is stirred for 16 hours at 20° C. It is then taken up in a 5% strength sodium bicarbonate solution (50 cc) and extracted with ethyl acetate (50 cc) and the organic phase is washed with a saturated sodium chloride solution (2×20 cc), dried over sodium sulphate and then concentrated to dryness under reduced pressure (20 mm Hg) at 20° C. 3-(2-Acetoxy-vinyl)-7-amino-2-benzhydryloxycarbonyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (E-form) (1.26 g) is obtained in the form of a crude red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04365062 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-8cec18a73e1e4fb9a93d3c72e1ade992 |
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| Source note | uspto-grants-1982_12 |
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