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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287176Generated: October 30, 2026

Pyridine → HCID 70561454, compound

https://huagongshe.com/reaction/2287176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 13019671HCID 13019671—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70561454HCID 70561454108.9%

Reaction Steps

To a solution of 5 g of benzyl α-(3ξ-carbomethoxy-7-oxo-4-oxa-2,6-diazabicyclo[3.2.0]heptan-6-yl)-α-isopropylideneacetate in 100 ml of tetrahydrofuran are dropwise added 1.82 ml of pyridine and a solution of 2.86 g of benzoyl chloride in 20 ml of tetrahydrofuran at 0° C. under nitrogen atmosphere. After 20 minutes, the reaction mixture is warmed up to room temperature. After additional 2 hours, the mixture is diluted with ice water and extracted with ethyl acetate. The extract is washed with an aqueous sodium sulfate and condensed under reduced pressure to yield 7.02 g of benzyl α-(3ξ-carbomethoxy-2-benzoyl-7-oxo-4-oxa-2,6-diazabicyclo[3.2.0]heptan-6-yl)-α-isopropylideneacetate as crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04269773
Source datasetuspto-grants-1981_05
ORD IDord-568a3cb40a264c8fb7d26a3ede5ddd22
Source noteuspto-grants-1981_05