HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198660Generated: October 26, 2026
Lithium azide → 4-Azidomethyl-2'-cyanobiphenyl
https://huagongshe.com/reaction/1198660
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium azide | HCID 88163 | — |
| Reactant | 4'-(Bromomethyl)-2-cyanobiphenyl | HCID 1501912 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Azidomethyl-2'-cyanobiphenyl | HCID 10353989 | — |
Reaction Steps
To a stirred suspension of 20 mmole of 4-bromomethyl-2'-cyanobiphenyl [P. E. Aldrich, M. E. Pierce, and J. J. V. Duncia, European Patent Application 291,969 (1988)] in 55 ml of dry DMSO was added 1.23 g (25 mmole) of freshly pulverized lithium azide, and the mixture was stirred at room temperature under N2. Within a few minutes virtually all of the solid had dissolved, accompanied by a mild exotherm, and this was followed immediately by precipitation of product. After 4 hours the solid was collected on a filter and washed with some methanol, then with a relatively large volume of H2O, and finally again with methanol. The solid was air-dried overnight and then dried further in a vacuum oven at 70° C. (<1 mm) to give white crystals, satisfactory purity by TLC (9:1 hexane-ethyl acetate) for use in the next step. From the combined filtrate and washes was recovered a less pure second crop (cream-colored crystals), which was also usable in the next step. Mass spectrum (FAB) m/e 235 (M+ +1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05281614 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-fe8ca6f818114b999c810469276387c3 |
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| Source note | uspto-grants-1994_01 |
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