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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730316Generated: November 1, 2026

Hydrochloric Acid → 6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penam

https://huagongshe.com/reaction/1730316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantSodium AzideHCID 33557—
ReactantHCID 70604454HCID 70604454—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penamHCID 178431921—

Reaction Steps

A mixture of 6-triphenylmethylamino-2,2-dimethyl-3-cyanopenam benzene solvate, (258 mg., 0.5 mmole), sodium azide (33 mg. 0.5 mmole), triethylamine hydrochloride (69 mg., 0.5 mmole) and chloroform (10 ml.) isstirred and heated to reflux for three hours. Sodium azide (0.5 mmole) is then added to the mixture and refluxing continued overnight. One equivalent of each of sodium azide and triethylamine hydrochloride are added to the mixture which is refluxed for an additional 2 hours. These additions are repeated twice more after which the mixture is again refluxed overnight. The mixture is cooled to room temperature and chloroform (10 ml.) added followed by water (10 ml.). The pH is adjusted to 2.0 with 6N hydrochloric acid, the mixture thoroughly mixed and the layers separated. The chloroform phase is washed with water (10 ml.) and is then seeded with a crystal from the product of Example 13. Crystallization occurs within five minutes. The slurry is stirred for ten minutes and then slowly added to an equal volume of hxane. The resulting slurry is stirred for 15 minutes and then filtered. The filter cake is washed with hexane and then air dried. Yield = 124 mg., 51.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03992394
Source datasetuspto-grants-1976_11
ORD IDord-03da952d1a824a93b00128137bd247a7
Source noteuspto-grants-1976_11