HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071861Generated: October 27, 2026
1-t-Butylazo-1-chlorocyclohexane → 1-t-Butylazo-1-phenylcyclohexane
https://huagongshe.com/reaction/2071861
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-t-Butylazo-1-chlorocyclohexane | HCID 23344784 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-t-Butylazo-1-phenylcyclohexane | HCID 20288890 | — |
Reaction Steps
To a clean, dry 250 ml. round bottom 4 neck flask equipped with a magnetic stirrer, thermometer, condenser and addition funnel, which was being purged with nitrogen, was added an ether solution containing 0.06 moles of phenyl-magnesium bromide. The solution was cooled to 5° C. and a solution of 8.7 g. (0.043 moles) of 1-t-butylazo-1-chlorocyclohexane in 50 ml. of ether was added dropwise over 1/2 hour. After the addition was complete, the reaction was stirred for 15 minutes at room temperature and the excess phenylmagnesium bromide destroyed by the addition of wet ether. The reaction mixture was poured into 200 ml. of cold water and the ether layer separated, washed with 5% HCl, saturated sodium bicarbonate solution, saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and the ether removed on a rotating evaporator leaving 9.75 g. (93%) of a yellow liquid. The infrared spectrum of the product was in agreement with the structure of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04048423 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-bb075f2eb8c64ea98d2e6eedf9b9aa63 |
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| Source note | uspto-grants-1977_09 |
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