HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679628Generated: October 30, 2026
Sodium Azide → 6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penam
https://huagongshe.com/reaction/1679628
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Piperidine, 1-methyl-, hydrochloride | HCID 205378 | — |
| Reactant | HCID 70604455 | HCID 70604455 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penam | HCID 178431921 | — |
Reaction Steps
A mixture of 6-triphenylmethylamino-2,2-dimethyl-3-cyanopenam (10 g. 0.0193 mole) 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 precipitate the 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04081455 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-7b2aa4cc354343bfa2112b4c0b6f6450 |
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| Source note | uspto-grants-1978_03 |
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