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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730319Generated: November 2, 2026

Sodium Azide → 6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penam

https://huagongshe.com/reaction/1730319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantPiperidine, 1-methyl-, hydrochlorideHCID 205378—
ReactantHCID 70604455HCID 70604455—
SolventChloroformHCID 6212—
Product6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penamHCID 178431921—

Reaction Steps

A mixture of 6-triphenylmethylamino-2,2-dimethyl-3-cyanopenam (10 g. 0.0193mole) sodium azide (7.41 g., 0.114 mole), N-methylpiperidine hydrochloride (3.39 g., 0.025 mole) and chloroform (100 ml.) is refluxed for four hours in a round-bottomed flask equipped with stirrer, condenser, and drying tube. The reaction mixture is then cooled and water (300 ml.) and chloroform (100 ml.) added. The mixture is thoroughly mixed, the chloroform layer separated and washed successively with 1N hydrochloric acid (100 ml.) and saturated brine (100 ml.). It is then filtered quickly through anhydrous sodium sulfate and concentrated under reduced pressure to about 75 ml. Hexane (20 ml.) is added to the concentrate to precipitatethe product as white crystals. The crystals are recovered by filtration, washed with 20% hexane-methylene chloride (50 ml.) and dried in vacuo at room temperature. Yield = 2.7 g. (29.6%) m.p. 133=136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03992394
Source datasetuspto-grants-1976_11
ORD IDord-2fb0a318e7ff4a20b35c0da018fe3ee0
Source noteuspto-grants-1976_11