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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730894Generated: November 1, 2026

Sodium Bicarbonate → HCID 70616087, compound

https://huagongshe.com/reaction/1730894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131710538HCID 131710538—
SolventDichloromethaneHCID 6344—
ProductHCID 70616087HCID 70616087—

Reaction Steps

A suspension of t-butyl 7β-amino-3-vinylceph-3-em-4-carboxylate hydrogen p-toluenesulphonate (1.14 g, 2.5 mmole) in methylene chloride (25 ml) was shaken with 4 percent aqueous sodium hydrogen carbonate solution (10 ml) until the organic phase cleared. The aqueous phase was re-extracted with methylene chloride (10 ml), and the combined organic phases were washed with water (10 ml) and dried (MgSO4). The solution of t-butyl 7β-amino-3-vinylceph-3-em-4-carboxylate so obtained was stirred and treated with a solution of dicyclohexylcarbodiimide (515 mg, 1 equiv.) in dry methylene chloride (10 ml). A solution of p-nitrophenylacetic acid (453 mg, 1 equiv.) in methylene chloride (15 ml) was added over a period of 5 minutes and the mixture was stirred at 30° for 2 hours. The precipitated N,N'-dicyclohexylurea was filtered off, and the filtrate was washed with 3%-sodium hydrogen carbonate solution (50 ml), water (50 ml), 2N-hydrochloric acid (25 ml) and water (25 ml), dried (MgSO4 ) and evaporated to an orange gelatinous solid. This solid was triturated with ethyl acetate (150 ml), the insoluble dicyclohexylurea was removed by filtration, and the filtrate was evaporated to give t-butyl 7β-(p-nitrophenylacetamido)-3-vinylceph-3-em-4-carboxylate (1.02 g, 92%) (see Table 1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994884
Source datasetuspto-grants-1976_11
ORD IDord-f37dfc2a29fc4cb69b0817f482d33e45
Source noteuspto-grants-1976_11