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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163655Generated: November 2, 2026

Pyridine → HCID 70604455, compound

https://huagongshe.com/reaction/2163655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosgeneHCID 6371—
ReactantHCID 70604248HCID 70604248—
SolventChloroformHCID 6212—
ProductHCID 70604455HCID 7060445567.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 6-triphenylmethylamino-2,2-dimethyl-3-carbamylpenam (11.01g., 0.024 mole), dry pyridine (4.9g., 0.062 mole) and dry chloroform (250 ml.) is stirred for five minutes and the resulting solution cooled to 0° C. in a wet ice/acetone bath. Phosgene (8.8 ml. of 3.41 molar solution in chloroform) is added by means of a syringe. The reaction mixture is stirred at 5° C. for ten minutes after which the cooling bath is removed and the reaction mixture allowed to warm to room temperature. It is stirred for 30 minutes and then washed successively with water (300 ml.), 1N hydrochloric acid (300 ml.), and water (300 ml.). The chloroform solution is dried (MgSO4), treated with activated charcoal, and filtered through diatomaceous earth. The filtrate is concentrated to reduced pressure and the residue taken up in methylene chloride (450 ml.). The methylene chloride solution is washed successively with 1N hydrochloric acid (150 ml.) and water (300 ml.) and then dried using anhydrous sodium sulfate. The dried solution is then filtered and concentrated under reduced pressure to give the product as a golden foam (7.1 g., 67.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04136096
Source datasetuspto-grants-1979_01
ORD IDord-b41dc7ea69e042d8ba121442190dc6ac
Source noteuspto-grants-1979_01