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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660396Generated: October 30, 2026

Sodium Bicarbonate → HCID 53643909, compound

https://huagongshe.com/reaction/1660396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 70554645HCID 70554645—
SolventAcetonitrileHCID 6342—
ProductHCID 53643909HCID 5364390993.3%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307230
Source datasetuspto-grants-1981_12
ORD IDord-863a0f70618c493a81363365f012aaac
Source noteuspto-grants-1981_12